The following data is part of a premarket notification filed by Intl. Immunoassay Laboratories, Inc. with the FDA for Embritrol Ck-mb Controls.
Device ID | K812671 |
510k Number | K812671 |
Device Name: | EMBRITROL CK-MB CONTROLS |
Classification | Enzyme Controls (assayed And Unassayed) |
Applicant | INTL. IMMUNOASSAY LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JJT |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-09-21 |
Decision Date | 1981-10-02 |