The following data is part of a premarket notification filed by Microanalytic Research, Inc. with the FDA for Mr1 Follitropin Ria Kit.
Device ID | K820740 |
510k Number | K820740 |
Device Name: | MR1 FOLLITROPIN RIA KIT |
Classification | Radioimmunoassay, Follicle-stimulating Hormone |
Applicant | MICROANALYTIC RESEARCH, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CGJ |
CFR Regulation Number | 862.1300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-03-18 |
Decision Date | 1982-04-06 |