510(k) K915208

FSH ENZYME IMMUNASSAY TEST KIT NO:KIF4057 by Medix Biotech, Inc. — Product Code CGJ

K915208 is an FDA 510(k) premarket notification submitted by Medix Biotech, Inc. for the device "FSH ENZYME IMMUNASSAY TEST KIT NO:KIF4057". The FDA issued a decision of Substantially Equivalent on December 18, 1991. The device falls under product code CGJ (Radioimmunoassay, Follicle-Stimulating Hormone), a Class I device regulated under 21 CFR 862.1300. Medix Biotech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 18, 1991
Date Received
November 18, 1991
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