510(k) K873534

OVUGEN SURETEST by Biogenex Laboratories — Product Code CEP

K873534 is an FDA 510(k) premarket notification submitted by Biogenex Laboratories for the device "OVUGEN SURETEST". The FDA issued a decision of Substantially Equivalent on November 23, 1987. The device falls under product code CEP (Radioimmunoassay, Luteinizing Hormone), a Class I device regulated under 21 CFR 862.1485. Biogenex Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 23, 1987
Date Received
September 1, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Luteinizing Hormone
Device Class
Class I
Regulation Number
862.1485
Review Panel
CH
Submission Type