510(k) K862813

FSH MAIACLONE IMMUNORADIOMETRIC ASSAY KIT by Serono Diagnostics, Inc. — Product Code CGJ

K862813 is an FDA 510(k) premarket notification submitted by Serono Diagnostics, Inc. for the device "FSH MAIACLONE IMMUNORADIOMETRIC ASSAY KIT". The FDA issued a decision of Substantially Equivalent on September 16, 1986. 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
September 16, 1986
Date Received
July 24, 1986
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