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 |