FUJIFILM EC-600WL v2
FUJIFILM EC-600WL v2 is a Class II device made by Fujifilm Corporation, cleared under FDA 510(k) K160196 on 23 Feb 2016 and listed in FDA GUDID since 21 Nov 2016 (UDI-DI 04547410337396), 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 | Number04547410337396 | Date21 Nov 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK160196 | Date23 Feb 2016 | StatusActive |
Official records
- AccessGUDID record 04547410337396
- FDA 510(k) database K160196
Across registries
- FDA 510(k) K160196 decided 23 Feb 2016 Active
- FDA GUDID UDI-DI 04547410337396 listed 21 Nov 2016 Listed
Timeline
- Cleared FDA 510(k) K160196
- Listed FDA GUDID 04547410337396
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Fujifilm
- Generic name
- Flexible video colonoscope, reusable
- Model / reference
- EC-600WL v2
- Primary DI / UDI-DI
- 04547410337396
- 510(k) Number
- FDA product code
- FDF
- GMDN term
- Flexible video colonoscope, reusable
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
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