Snowden-Pencer 89-0501
Snowden-Pencer 89-0501 (890501) is a Class II device made by Steris Corporation, cleared under FDA 510(k) K110257 on 6 May 2011 and listed in FDA GUDID since 28 Mar 2018 (UDI-DI 10885403155499), 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 | Number10885403155499 | Date28 Mar 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK110257 | Date6 May 2011 | StatusActive |
Official records
- AccessGUDID record 10885403155499
- FDA 510(k) database K110257
Across registries
- FDA 510(k) K110257 decided 6 May 2011 Active
- FDA GUDID UDI-DI 10885403155499 listed 28 Mar 2018 Listed
Timeline
- Cleared FDA 510(k) K110257
- Listed FDA GUDID 10885403155499
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Snowden-Pencer
- Generic name
- Rigid endoscopic tissue manipulation forceps, reusable
- Model / Ref / Catalog
- 89-0501, 890501
- Primary DI / UDI-DI
- 10885403155499
- 510(k) Number
- FDA product code
- GCJ
- GMDN term
- Rigid endoscopic tissue manipulation forceps, reusable
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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