Delasco Bipolar Forceps 26404
by Dermatologic Lab and Supply, Inc.
Delasco Bipolar Forceps 26404 is a Class II device made by Dermatologic Lab and Supply, Inc., cleared under FDA 510(k) K964176 on 14 Aug 1997 and listed in FDA GUDID since 10 Jul 2018 (UDI-DI 00609960000459), 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 | Number00609960000459 | Date10 Jul 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK964176 | Date14 Aug 1997 | StatusActive |
Official records
- AccessGUDID record 00609960000459
- FDA 510(k) database K964176
Across registries
- FDA 510(k) K964176 decided 14 Aug 1997 Active
- FDA GUDID UDI-DI 00609960000459 listed 10 Jul 2018 Listed
Timeline
- Cleared FDA 510(k) K964176
- Listed FDA GUDID 00609960000459
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Delasco Bipolar Forceps
- Generic name
- Endoscopic electrosurgical electrode, bipolar, reusable
- Model / Ref / Catalog
- 26404
- Primary DI / UDI-DI
- 00609960000459
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Endoscopic electrosurgical electrode, bipolar, reusable
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Endoscopic electrosurgical electrode, bipolar, reusable.