Bovie AA90
by Aspen Surgical Products, Inc. 4 variants
Bovie AA90 is a Class II device made by Aspen Surgical Products, Inc., cleared under FDA 510(k) K945493 on 30 Jan 1995 and listed in FDA GUDID since 28 Aug 2024 (UDI-DI 10887482177508), 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 | Number10887482177508 | Date28 Aug 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK945493 | Date30 Jan 1995 | StatusActive |
Official records
- AccessGUDID record 10887482177508
- FDA 510(k) database K945493
Across registries
- FDA 510(k) K945493 decided 30 Jan 1995 Active
- FDA GUDID UDI-DI 10887482177508 listed 28 Aug 2024 Listed
Timeline
- Cleared FDA 510(k) K945493
- Listed FDA GUDID 10887482177508
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Bovie
- Generic name
- Electrocautery system generator, battery-powered
- Model / reference
- AA90
- Primary DI / UDI-DI
- 10887482177508
- 510(k) Number
- FDA product code
- HQP
- GMDN term
- Electrocautery system generator, battery-powered
- Device class
- Class II
- Regulation number
- 886.4115
- GUDID distribution status
- In Commercial Distribution