ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY— 510(k) K935781
UnknownSherwood Medical Co.
FDA 510(k) clearance K935781 for ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY, Unknown on 1995-01-27. Applicant: Sherwood Medical Co.. Device class: 2.
Clearance details
- Applicant
- Sherwood Medical Co.
- Product code
- Code FEG
- Device class
- Class 2
- Regulation
- 21 CFR 876.5980
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- St. Louis, MO, US
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- K960677 — KANGAROO JEJUNAL FEEDING SYSTEM
Adverse events under product code FEG
product code FEG- Death
- 2
- Total
- 2
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 →
Data sourced from openFDA. This site is unofficial and independent of the FDA.