The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Elecsys Fsh Assay.
Device ID | K964693 |
510k Number | K964693 |
Device Name: | ELECSYS FSH ASSAY |
Classification | Radioimmunoassay, Follicle-stimulating Hormone |
Applicant | BOEHRINGER MANNHEIM CORP. 2400 BISSO LN. Concord, CA 94524 |
Contact | Betsy Soares-maddox |
Correspondent | Betsy Soares-maddox BOEHRINGER MANNHEIM CORP. 2400 BISSO LN. Concord, CA 94524 |
Product Code | CGJ |
CFR Regulation Number | 862.1300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-11-22 |
Decision Date | 1996-12-16 |
Summary: | summary |