The following data is part of a premarket notification filed by Professional Medical Services with the FDA for Pms Angio Drape.
| Device ID | K890471 |
| 510k Number | K890471 |
| Device Name: | PMS ANGIO DRAPE |
| Classification | Drape, Surgical |
| Applicant | PROFESSIONAL MEDICAL SERVICES P.O. BOX 250 700 WEST 200 NORTH North Salt Lake, UT 84054 |
| Contact | James E Williams |
| Correspondent | James E Williams PROFESSIONAL MEDICAL SERVICES P.O. BOX 250 700 WEST 200 NORTH North Salt Lake, UT 84054 |
| Product Code | KKX |
| CFR Regulation Number | 878.4370 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-31 |
| Decision Date | 1989-02-27 |