00711203
00711203 is a Class II device made by US Endoscopy, cleared under FDA 510(k) K924106 on 24 Nov 1992 and listed in FDA GUDID since 19 Mar 2020 (UDI-DI 00724995183691), active (FDA 510(k)), not in commercial distribution (GUDID) as of 22 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 | Number00724995183691 | Date19 Mar 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK924106 | Date24 Nov 1992 | StatusActive |
Official records
- AccessGUDID record 00724995183691
- FDA 510(k) database K924106
Across registries
- FDA 510(k) K924106 decided 24 Nov 1992 Active
- FDA GUDID UDI-DI 00724995183691 listed 19 Mar 2020 Listed
Timeline
- Cleared FDA 510(k) K924106
- Listed FDA GUDID 00724995183691
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Flexible endoscopic biopsy forceps, single-use
- Model / Ref / Catalog
- 00711203
- Primary DI / UDI-DI
- 00724995183691
- 510(k) Number
- FDA product code
- KNW
- GMDN term
- Flexible endoscopic biopsy forceps, single-use
- Device class
- Class II
- Regulation number
- 876.1075
- GUDID distribution status
- Not in Commercial Distribution
- Size
- Outer Diameter — 2.3 MillimeterLength — 160 Centimeter
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