The following data is part of a premarket notification filed by Medrad, Inc. with the FDA for Medrad Phased Array 1.5t Shoulder Imaging Surface Coil.
| Device ID | K960901 |
| 510k Number | K960901 |
| Device Name: | MEDRAD PHASED ARRAY 1.5T SHOULDER IMAGING SURFACE COIL |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Applicant | MEDRAD, INC. 14 MEDRAD DR. Indianola, PA 15051 -0780 |
| Contact | Rodney J Rylands |
| Correspondent | Rodney J Rylands MEDRAD, INC. 14 MEDRAD DR. Indianola, PA 15051 -0780 |
| Product Code | LNH |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-03-05 |
| Decision Date | 1996-05-29 |
| Summary: | summary |