Aed 5700C-S
by National Advanced Endoscopy Devices, Inc.
Aed 5700C-S 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 24 Nov 2017 (UDI-DI 00848657019323), 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 | Number00848657019323 | Date24 Nov 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK991656 | Date2 Dec 1999 | StatusActive |
Official records
- AccessGUDID record 00848657019323
- FDA 510(k) database K991656
Across registries
- FDA 510(k) K991656 decided 2 Dec 1999 Active
- FDA GUDID UDI-DI 00848657019323 listed 24 Nov 2017 Listed
Timeline
- Cleared FDA 510(k) K991656
- Listed FDA GUDID 00848657019323
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- Withdrawn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
- 5700C-S
- Primary DI / UDI-DI
- 00848657019323
- 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
- Sterilisation method
- Hydrogen Peroxide
Similar devices in this category
Other devices filed under Rigid optical arthroscope, reusable.
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