510(k) K791835

CORALENT COAT 125I CORTISOL RADIOIMM. by Radioassay Systems Laboratories, Inc. — Product Code CGR

K791835 is an FDA 510(k) premarket notification submitted by Radioassay Systems Laboratories, Inc. for the device "CORALENT COAT 125I CORTISOL RADIOIMM.". The FDA issued a decision of Substantially Equivalent on September 27, 1979. The device falls under product code CGR (Radioimmunoassay, Cortisol), a Class II device regulated under 21 CFR 862.1205. Radioassay Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 27, 1979
Date Received
September 17, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Cortisol
Device Class
Class II
Regulation Number
862.1205
Review Panel
CH
Submission Type