The following data is part of a premarket notification filed by Ssi Medical Services, Inc. with the FDA for Clinitron C-10.
| Device ID | K914351 |
| 510k Number | K914351 |
| Device Name: | CLINITRON C-10 |
| Classification | Table, Radiographic, Stationary Top |
| Applicant | SSI MEDICAL SERVICES, INC. BURDITT RADZIUS CHARTERED 333 W.WACKER DR.SUITE 2600 Chicago, IL 60606 |
| Contact | John F.lemker |
| Correspondent | John F.lemker SSI MEDICAL SERVICES, INC. BURDITT RADZIUS CHARTERED 333 W.WACKER DR.SUITE 2600 Chicago, IL 60606 |
| Product Code | IXQ |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-09-27 |
| Decision Date | 1992-02-14 |