The following data is part of a premarket notification filed by Cimarron Instruments, Inc. with the FDA for Cimarron 1000 Or 1000-2.
| Device ID | K790293 |
| 510k Number | K790293 |
| Device Name: | CIMARRON 1000 OR 1000-2 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | CIMARRON INSTRUMENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-02-08 |
| Decision Date | 1979-04-12 |