510(k) K894761

TANDEM-E FSH IMMUNOENZYMETRIC ASSAY KIT by Hybritech, Inc. — Product Code CGJ

K894761 is an FDA 510(k) premarket notification submitted by Hybritech, Inc. for the device "TANDEM-E FSH IMMUNOENZYMETRIC ASSAY KIT". The FDA issued a decision of Substantially Equivalent on September 13, 1989. 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
September 13, 1989
Date Received
July 27, 1989
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