RUSH ORAL/NASAL TRACHEAL TUBE CUFFED MAGILL/MURPHY— 510(k) K961837
Substantially EquivalentRusch Intl.
FDA 510(k) clearance K961837 for RUSH ORAL/NASAL TRACHEAL TUBE CUFFED MAGILL/MURPHY, Substantially Equivalent on 1996-08-16. Applicant: Rusch Intl.. Device class: 2.
Clearance details
- Applicant
- Rusch Intl.
- Product code
- Code BTR
- Device class
- Class 2
- Regulation
- 21 CFR 868.5730
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jeffrey, NH, US
Recent devices under product code BTR
view all- K251794 — Tenax® Laser Resistant Endotracheal Tube
- K253437 — Spiro-VISTA
- K250173 — Shiley Oral RAE Tracheal Tube Cuffless, Murphy Eye (113-XX) Shiley Nasal RAE Tracheal Tube Cuffless, Murphy Eye (114-XX) Shiley Oral RAE Tracheal Tube Cuffed, Murphy Eye (115-XX) Shiley Oral RAE Tracheal Tube with TaperGuard Cuff, Murphy Eye (115-XXOR) Shiley Nasal RAE Tracheal Tube with TaperGuard Cuff, Murphy Eye (119-XXNR)
- K243785 — Shiley Oral/Nasal Tracheal Tube with TaperGuard Cuff Reinforced, Murphy Eye Shiley Tracheal Tube TaperGuard Cuff Reinforced with Stylet Shiley Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced Shiley Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced, Murphy Eye Shiley Oral/Nasal Tracheal Tube Cuffless Reinforced
- K243579 — AeroJet Ventilation Catheter
More clearances from Rusch Intl.
view allAdverse events under product code BTR
product code BTR- Death
- 92
- Injury
- 1,263
- Malfunction
- 7,475
- Other
- 2
- Total
- 8,832
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K961837
K-number listed on FDA's recall record- Z-1845-2023 — Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504550
- Z-1846-2023 — Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504555
- Z-1847-2023 — Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504560
- Z-1848-2023 — Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504565
- Z-1849-2023 — Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504570
- Z-1850-2023 — Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504575
- Z-1851-2023 — Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504580
- Z-1852-2023 — Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504585
- Z-1853-2023 — Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504590
- Z-1881-2023 — Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080055
- Z-1882-2023 — Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080095
- Z-1883-2023 — Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080100
- Z-1884-2023 — Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050
- Z-1885-2023 — Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082055
- Z-1886-2023 — Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082060
- Z-1887-2023 — Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082065
- Z-1888-2023 — Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070
- Z-1889-2023 — Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082075
- Z-1890-2023 — Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080
- Z-1891-2023 — Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082085
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K961837.
Data sourced from openFDA. This site is unofficial and independent of the FDA.