The following data is part of a premarket notification filed by Ohio Imaging, Inc. with the FDA for Prism 3000 Nuclear Gamma Camera System Modification.
| Device ID | K934722 |
| 510k Number | K934722 |
| Device Name: | PRISM 3000 NUCLEAR GAMMA CAMERA SYSTEM MODIFICATION |
| Classification | System, Tomography, Computed, Emission |
| Applicant | OHIO IMAGING, INC. 23060 MILES RD. Bedford Heights, OH 44128 |
| Contact | Norman J Yager |
| Correspondent | Norman J Yager OHIO IMAGING, INC. 23060 MILES RD. Bedford Heights, OH 44128 |
| Product Code | KPS |
| CFR Regulation Number | 892.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-09-29 |
| Decision Date | 1994-05-13 |