Snowden-Pencer SP83
Snowden-Pencer SP83 is a Class II device made by Steris Corporation, cleared under FDA 510(k) K991928 on 25 Jun 1999 and listed in FDA GUDID since 28 Mar 2018 (UDI-DI 10885403171451), 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 | Number10885403171451 | Date28 Mar 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK991928 | Date25 Jun 1999 | StatusActive |
Official records
- AccessGUDID record 10885403171451
- FDA 510(k) database K991928
Across registries
- FDA 510(k) K991928 decided 25 Jun 1999 Active
- FDA GUDID UDI-DI 10885403171451 listed 28 Mar 2018 Listed
Timeline
- Cleared FDA 510(k) K991928
- Listed FDA GUDID 10885403171451
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Snowden-Pencer
- Generic name
- Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
- Model / Ref / Catalog
- SP83
- Primary DI / UDI-DI
- 10885403171451
- 510(k) Number
- FDA product code
- GCJ
- GMDN term
- Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Endoscopic electrosurgical handpiece/electrode, monopolar, reusable.