510(k) K870520

TANDEM(R)-M FSH IMMUNOENZYMETRIC ASSAY by Hybritech, Inc. — Product Code CGJ

K870520 is an FDA 510(k) premarket notification submitted by Hybritech, Inc. for the device "TANDEM(R)-M FSH IMMUNOENZYMETRIC ASSAY". The FDA issued a decision of Substantially Equivalent on March 10, 1987. The device falls under product code CGJ (Radioimmunoassay, Follicle-Stimulating Hormone), a Class I device regulated under 21 CFR 862.1300. Hybritech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 10, 1987
Date Received
February 6, 1987
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