510(k) K823476

GAMMADAB LH RADIO-KIT #CA-1508 by Clinical Assays, Inc. — Product Code CEP

K823476 is an FDA 510(k) premarket notification submitted by Clinical Assays, Inc. for the device "GAMMADAB LH RADIO-KIT #CA-1508". The FDA issued a decision of Substantially Equivalent on December 28, 1982. The device falls under product code CEP (Radioimmunoassay, Luteinizing Hormone), a Class I device regulated under 21 CFR 862.1485. Clinical Assays, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 28, 1982
Date Received
November 22, 1982
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