Oasis MV-663
by American Health Service Sales Corporation
Oasis MV-663 is a Class II device made by American Health Service Sales Corporation, cleared under FDA 510(k) K080684 on 9 Jun 2008 and listed in FDA GUDID since 14 Jan 2016 (UDI-DI B031MV6630), 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 | NumberB031MV6630 | Date14 Jan 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK080684 | Date9 Jun 2008 | StatusActive |
Official records
- FDA 510(k) database K080684
Across registries
- FDA 510(k) K080684 decided 9 Jun 2008 Active
- FDA GUDID UDI-DI B031MV6630 listed 14 Jan 2016 Listed
Timeline
- Cleared FDA 510(k) K080684
- Listed FDA GUDID B031MV6630
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Oasis
- Generic name
- Nylon suture, non-bioabsorbable, monofilament
- Model / reference
- MV-663
- Primary DI / UDI-DI
- B031MV6630
- 510(k) Number
- FDA product code
- GAR
- GMDN term
- Nylon suture, non-bioabsorbable, monofilament
- Device class
- Class II
- Regulation number
- 878.5020
- GUDID distribution status
- In Commercial Distribution
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