VV-Plug 667145-303
by Oscor Inc.
VV-Plug 667145-303 is a Class II device made by Oscor Inc., cleared under FDA 510(k) K031164 on 19 Jun 2003 and listed in FDA GUDID since 1 Jun 2026 (UDI-DI 00885672013226), active as of 22 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 | Number00885672013226 | Date1 Jun 2026 | StatusListed |
| United States | FDA 510(k)ST | NumberK031164 | Date19 Jun 2003 | StatusActive |
Official records
- AccessGUDID record 00885672013226
- FDA 510(k) database K031164
Across registries
- FDA 510(k) K031164 decided 19 Jun 2003 Active
- FDA GUDID UDI-DI 00885672013226 listed 1 Jun 2026 Listed
Timeline
- Cleared FDA 510(k) K031164
- Listed FDA GUDID 00885672013226
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- VV-Plug
- Generic name
- Implantable pulse generator port plug
- Model / Ref / Catalog
- 667145-303, VV-PLUG
- Primary DI / UDI-DI
- 00885672013226
- 510(k) Number
- FDA product code
- DTD
- GMDN term
- Implantable pulse generator port plug
- Device class
- Class II
- Regulation number
- 870.3620
- GUDID distribution status
- In Commercial Distribution
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