Lens 72204901
Lens 72204901 is a Class II device made by Smith & Nephew, Inc., cleared under FDA 510(k) K153606 on 2 Jun 2016 and listed in FDA GUDID since 12 Sep 2016 (UDI-DI 00885556618110), 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 | Number00885556618110 | Date12 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK153606 | Date2 Jun 2016 | StatusActive |
Official records
- AccessGUDID record 00885556618110
- FDA 510(k) database K153606
Across registries
- FDA 510(k) K153606 decided 2 Jun 2016 Active
- FDA GUDID UDI-DI 00885556618110 listed 12 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K153606
- Listed FDA GUDID 00885556618110
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lens
- Generic name
- Endoscopic video imaging system
- Model / Ref / Catalog
- 72204901
- Description
- KIT NORWEGIAN LENS INTEGRATED SYSTEM NON-WIFI
- Primary DI / UDI-DI
- 00885556618110
- 510(k) Number
- FDA product code
- GCJ
- GMDN term
- Endoscopic video imaging system
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
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