The following data is part of a premarket notification filed by Medical Metrics, Inc. with the FDA for Kimax Qma.
| Device ID | K022585 |
| 510k Number | K022585 |
| Device Name: | KIMAX QMA |
| Classification | System, Image Processing, Radiological |
| Applicant | MEDICAL METRICS, INC. 10540 ROCKELY RD. SUITE 200 Houston, TX 77099 |
| Contact | Mark Lamp |
| Correspondent | Mark Lamp MEDICAL METRICS, INC. 10540 ROCKELY RD. SUITE 200 Houston, TX 77099 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-08-05 |
| Decision Date | 2002-10-11 |