The following data is part of a premarket notification filed by Cox Medical Ent., Inc. with the FDA for Thermal Option.
| Device ID | K932790 |
| 510k Number | K932790 |
| Device Name: | THERMAL OPTION |
| Classification | Forceps, Biopsy, Electric |
| Applicant | COX MEDICAL ENT., INC. 2186 EASTMAN AVE. SUITE 110 Ventura, CA 93003 |
| Contact | Lanita Cox |
| Correspondent | Lanita Cox COX MEDICAL ENT., INC. 2186 EASTMAN AVE. SUITE 110 Ventura, CA 93003 |
| Product Code | KGE |
| CFR Regulation Number | 876.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-09 |
| Decision Date | 1994-01-28 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10350770924981 | K932790 | 000 |
| 10350770924967 | K932790 | 000 |
| 10350770924943 | K932790 | 000 |
| 10350770924912 | K932790 | 000 |
| 10350770924905 | K932790 | 000 |
| 10350770924882 | K932790 | 000 |
| 10350770924875 | K932790 | 000 |
| 10350770924868 | K932790 | 000 |
| 10350770924844 | K932790 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() THERMAL OPTION 98182548 not registered Live/Pending |
STURDI PRODUCTS COMPANY 2023-09-15 |
![]() THERMAL OPTION 74399405 1912396 Live/Registered |
AVENT, INC. 1993-06-04 |