DUAL-TROL
Electrosurgical, Cutting & Coagulation & Accessories
CIMARRON INSTRUMENTS, INC.
The following data is part of a premarket notification filed by Cimarron Instruments, Inc. with the FDA for Dual-trol.
Pre-market Notification Details
| Device ID | K802972 |
| 510k Number | K802972 |
| Device Name: | DUAL-TROL |
| 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 | 1980-11-21 |
| Decision Date | 1981-01-15 |
Trademark Results [DUAL-TROL]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DUAL-TROL 73165145 1121372 Dead/Expired |
CIMARRON INSTRUMENTS, INC. 1978-04-05 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.