The following data is part of a premarket notification filed by Cox Sterile Products, Inc. with the FDA for Disinfection With The Cox Dry Heat Sterilizer.
| Device ID | K910925 |
| 510k Number | K910925 |
| Device Name: | DISINFECTION WITH THE COX DRY HEAT STERILIZER |
| Classification | Sterilizer, Dry Heat |
| Applicant | COX STERILE PRODUCTS, INC. 5115 MCKINNEY AVENUE, SUITE C Dallas, TX 75205 |
| Contact | Keith Cox |
| Correspondent | Keith Cox COX STERILE PRODUCTS, INC. 5115 MCKINNEY AVENUE, SUITE C Dallas, TX 75205 |
| Product Code | KMH |
| CFR Regulation Number | 880.6870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-03-05 |
| Decision Date | 1992-05-08 |