The following data is part of a premarket notification filed by Technical Resources, Inc. with the FDA for Blade, Handle, Scalpel Forceps, Surgery.
| Device ID | K810572 |
| 510k Number | K810572 |
| Device Name: | BLADE, HANDLE, SCALPEL FORCEPS, SURGERY |
| Classification | Blade, Scalpel |
| Applicant | TECHNICAL RESOURCES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GES |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-03-03 |
| Decision Date | 1981-03-20 |