The following data is part of a premarket notification filed by Santa Barbara Medco, Inc. with the FDA for Rk Iv Surgical Blades.
| Device ID | K812071 |
| 510k Number | K812071 |
| Device Name: | RK IV SURGICAL BLADES |
| Classification | Blade, Scalpel |
| Applicant | SANTA BARBARA MEDCO, 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 | 1981-07-21 |
| Decision Date | 1981-08-31 |