The following data is part of a premarket notification filed by Jpi, Inc. with the FDA for Jpi X-ray Film Cassette.
| Device ID | K930244 |
| 510k Number | K930244 |
| Device Name: | JPI X-RAY FILM CASSETTE |
| Classification | Cassette, Radiographic Film |
| Applicant | JPI, INC. 350-J CENTRAL AVE. Bohemia, NY 11716 |
| Contact | Wiliam Hague |
| Correspondent | Wiliam Hague JPI, INC. 350-J CENTRAL AVE. Bohemia, NY 11716 |
| Product Code | IXA |
| CFR Regulation Number | 892.1850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-01-19 |
| Decision Date | 1993-04-07 |