510(k) K964693

ELECSYS FSH ASSAY by Boehringer Mannheim Corp. — Product Code CGJ

K964693 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "ELECSYS FSH ASSAY". The FDA issued a decision of Substantially Equivalent on December 16, 1996. The device falls under product code CGJ (Radioimmunoassay, Follicle-Stimulating Hormone), a Class I device regulated under 21 CFR 862.1300. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 16, 1996
Date Received
November 22, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Follicle-Stimulating Hormone
Device Class
Class I
Regulation Number
862.1300
Review Panel
CH
Submission Type