VASCLIP
FDA 510(k) clearance K021745 · decided 2002-08-20
Clearance details
- K-number
- K021745
- Device name
- VASCLIP
- Applicant
- Vmbc, LLC
- Decision
- Unknown
- Date received
- 2002-05-28
- Decision date
- 2002-08-20
- Days to decision
- 84 days
- Clearance type
- Traditional
- Product code
- NJC
- Device class
- 2
- Regulation number
- 878.4300
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- White Bear Lake, MN, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| TI CLIP APPLIER (K034029) | Gyrx, LLC | 2004-03-05 |
Recalls involving this device
No recalls on record reference this clearance.