The following data is part of a premarket notification filed by Precise Optics with the FDA for P1806 Mobile C-arm Image Intensifier.
| Device ID | K792225 |
| 510k Number | K792225 |
| Device Name: | P1806 MOBILE C-ARM IMAGE INTENSIFIER |
| Classification | System, X-ray, Fluoroscopic, Image-intensified |
| Applicant | PRECISE OPTICS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JAA |
| CFR Regulation Number | 892.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-11-05 |
| Decision Date | 1979-12-20 |