Geiger Thermal Cautery Unit 150-S
by Dermatologic Lab and Supply, Inc.
Geiger Thermal Cautery Unit 150-S is a Class II device made by Dermatologic Lab and Supply, Inc., cleared under FDA 510(k) K002341 on 23 Oct 2000 and listed in FDA GUDID since 10 Jul 2018 (UDI-DI 00609960000787), 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 | Number00609960000787 | Date10 Jul 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK002341 | Date23 Oct 2000 | StatusActive |
Official records
- AccessGUDID record 00609960000787
- FDA 510(k) database K002341
Across registries
- FDA 510(k) K002341 decided 23 Oct 2000 Active
- FDA GUDID UDI-DI 00609960000787 listed 10 Jul 2018 Listed
Timeline
- Cleared FDA 510(k) K002341
- Listed FDA GUDID 00609960000787
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Geiger Thermal Cautery Unit
- Generic name
- Electrocautery system generator, line-powered
- Model / Ref / Catalog
- 150-S
- Primary DI / UDI-DI
- 00609960000787
- 510(k) Number
- FDA product code
- HQO
- GMDN term
- Electrocautery system generator, line-powered
- Device class
- Class II
- Regulation number
- 886.4115
- GUDID distribution status
- In Commercial Distribution