Aed 5700B-Wlf
by National Advanced Endoscopy Devices, Inc.
Aed 5700B-Wlf is a Class II device made by National Advanced Endoscopy Devices, Inc., cleared under FDA 510(k) K991656 on 2 Dec 1999 and listed in FDA GUDID since 22 May 2019 (UDI-DI 00848657074711), 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 | Number00848657074711 | Date22 May 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK991656 | Date2 Dec 1999 | StatusActive |
Official records
- AccessGUDID record 00848657074711
- FDA 510(k) database K991656
Across registries
- FDA 510(k) K991656 decided 2 Dec 1999 Active
- FDA GUDID UDI-DI 00848657074711 listed 22 May 2019 Listed
Timeline
- Cleared FDA 510(k) K991656
- Listed FDA GUDID 00848657074711
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Aed
- Generic name
- Rigid optical arthroscope, reusable
- Model / reference
- 5700B-WLF
- Primary DI / UDI-DI
- 00848657074711
- 510(k) Number
- FDA product code
- HRX
- GMDN term
- Rigid optical arthroscope, reusable
- Device class
- Class II
- Regulation number
- 888.1100
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Rigid optical arthroscope, reusable.
Other devices from National Advanced Endoscopy Devices, Inc.
See all devices from National Advanced Endoscopy Devices, Inc. →