The following data is part of a premarket notification filed by Arnold & Richter Cine Technik with the FDA for Arripro 35 St/tv.
| Device ID | K973115 |
| 510k Number | K973115 |
| Device Name: | ARRIPRO 35 ST/TV |
| Classification | Illuminator, Radiographic-film |
| Applicant | ARNOLD & RICHTER CINE TECHNIK TURKENSTRASSE 89 Munich, DE 80799 |
| Contact | Thomas Popp |
| Product Code | IXC |
| CFR Regulation Number | 892.1890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 1997-08-20 |
| Decision Date | 1997-09-02 |
| Summary: | summary |