The following data is part of a premarket notification filed by J.p.i. Chicago Co. with the FDA for X-ray Grid (radiological Grid).
| Device ID | K940309 |
| 510k Number | K940309 |
| Device Name: | X-RAY GRID (RADIOLOGICAL GRID) |
| Classification | Grid, Radiographic |
| Applicant | J.P.I. CHICAGO CO. 2451 UNITE LN. ELK GROVE, IL 60007 |
| Contact | JAMES E OGRADY |
| Correspondent | JAMES E OGRADY J.P.I. CHICAGO CO. 2451 UNITE LN. ELK GROVE, IL 60007 |
| Product Code | IXJ |
| CFR Regulation Number | 892.1910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-01-24 |
| Decision Date | 1994-04-22 |