The following data is part of a premarket notification filed by Cimarron Instruments, Inc. with the FDA for Disposable Skin Retractor.
| Device ID | K801151 |
| 510k Number | K801151 |
| Device Name: | DISPOSABLE SKIN RETRACTOR |
| Classification | Retractor, Self-retaining, For Neurosurgery |
| Applicant | CIMARRON INSTRUMENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GZT |
| CFR Regulation Number | 882.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-05-13 |
| Decision Date | 1980-05-20 |