The following data is part of a premarket notification filed by The Owenby Co. with the FDA for P.s.m. Surgical Hood.
| Device ID | K761070 |
| 510k Number | K761070 |
| Device Name: | P.S.M. SURGICAL HOOD |
| Classification | Hood, Surgical |
| Applicant | THE OWENBY CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FXY |
| CFR Regulation Number | 878.4040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-11-16 |
| Decision Date | 1976-12-30 |