The following data is part of a premarket notification filed by Tecnomed, Inc. with the FDA for Plurimat;radiographic Tube Mount.
| Device ID | K781065 |
| 510k Number | K781065 |
| Device Name: | PLURIMAT;RADIOGRAPHIC TUBE MOUNT |
| Classification | Tube Mount, X-ray, Diagnostic |
| Applicant | TECNOMED, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IYB |
| CFR Regulation Number | 892.1770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-06-26 |
| Decision Date | 1978-07-17 |