The following data is part of a premarket notification filed by Surgikos, Inc. with the FDA for Surgical Corp..
| Device ID | K760861 |
| 510k Number | K760861 |
| Device Name: | SURGICAL CORP. |
| Classification | Cap, Surgical |
| Applicant | SURGIKOS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FYF |
| CFR Regulation Number | 878.4040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-10-18 |
| Decision Date | 1976-11-03 |