VENOJECT LUER ADAPTER— 510(k) K041358
Substantially EquivalentTerumo Europe N.V.
FDA 510(k) clearance K041358 for VENOJECT LUER ADAPTER, Substantially Equivalent on 2004-05-28. Applicant: Terumo Europe N.V.. Device class: 2.
Clearance details
- Applicant
- Terumo Europe N.V.
- Product code
- Code JKA
- Device class
- Class 2
- Regulation
- 21 CFR 862.1675
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Elkton, MD, US
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More clearances from Terumo Europe N.V.
view allAdverse events under product code JKA
product code JKA- Injury
- 455
- Malfunction
- 26,686
- Other
- 4
- Total
- 27,145
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.