The following data is part of a premarket notification filed by Nuclear Medical Laboratories, Inc. with the FDA for Diagnostic Radioimmunoassay For Quanti.
| Device ID | K822298 |
| 510k Number | K822298 |
| Device Name: | DIAGNOSTIC RADIOIMMUNOASSAY FOR QUANTI |
| Classification | Acid Phosphatase (prostatic), Tartrate Inhibited |
| Applicant | NUCLEAR MEDICAL LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JFH |
| CFR Regulation Number | 862.1020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-08-03 |
| Decision Date | 1982-09-02 |