Vas-Q-Clip 2233
Vas-Q-Clip 2233 is a Class II device made by Nanova Biomaterials Inc, cleared under FDA 510(k) K151943 on 25 Mar 2016 and listed in FDA GUDID since 1 Jul 2016 (UDI-DI 10816537020025), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10816537020025 | Date1 Jul 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK151943 | Date25 Mar 2016 | StatusActive |
Official records
- AccessGUDID record 10816537020025
- FDA 510(k) database K151943
Across registries
- FDA 510(k) K151943 decided 25 Mar 2016 Active
- FDA GUDID UDI-DI 10816537020025 listed 1 Jul 2016 Listed
Timeline
- Cleared FDA 510(k) K151943
- Listed FDA GUDID 10816537020025
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vas-Q-Clip
- Generic name
- Ligation clip, synthetic polymer, non-bioabsorbable
- Model / Ref / Catalog
- 2233
- Primary DI / UDI-DI
- 10816537020025
- 510(k) Number
- FDA product code
- FZP
- GMDN term
- Ligation clip, synthetic polymer, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 878.4300
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
- MRI safety
- MR Safe
- Size
- Height — 12.68 Millimeter