The following data is part of a premarket notification filed by Jpi, Inc. with the FDA for Jpi Aluminum Interspaced X-ray Grid.
| Device ID | K926261 |
| 510k Number | K926261 |
| Device Name: | JPI ALUMINUM INTERSPACED X-RAY GRID |
| Classification | Grid, Radiographic |
| Applicant | JPI, INC. 350-J CENTRAL AVE. Bohemia, NY 11716 |
| Contact | William Hague |
| Correspondent | William Hague JPI, INC. 350-J CENTRAL AVE. Bohemia, NY 11716 |
| Product Code | IXJ |
| CFR Regulation Number | 892.1910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-12-18 |
| Decision Date | 1993-03-18 |