The following data is part of a premarket notification filed by Intl. Immunoassay Laboratories, Inc. with the FDA for Aburia-ck Ria Test Kit.
| Device ID | K813087 |
| 510k Number | K813087 |
| Device Name: | ABURIA-CK RIA TEST KIT |
| Classification | Fluorometric Method, Cpk Or Isoenzymes |
| Applicant | INTL. IMMUNOASSAY LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JHX |
| CFR Regulation Number | 862.1215 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-11-02 |
| Decision Date | 1981-12-17 |