510(k) K872627

FSH SEROZYME IMMUNOENZYMETRIC ASSAY KIT/MAG SEP PH by Serono Diagnostics, Inc. — Product Code CGJ

K872627 is an FDA 510(k) premarket notification submitted by Serono Diagnostics, Inc. for the device "FSH SEROZYME IMMUNOENZYMETRIC ASSAY KIT/MAG SEP PH". The FDA issued a decision of Substantially Equivalent on July 21, 1987. The device falls under product code CGJ (Radioimmunoassay, Follicle-Stimulating Hormone), a Class I device regulated under 21 CFR 862.1300. Serono Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 21, 1987
Date Received
July 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