510(k) K841641

CORNING MAGIC CORTISOL RADIOIMMUNO by Corning Medical & Scientific — Product Code CGR

K841641 is an FDA 510(k) premarket notification submitted by Corning Medical & Scientific for the device "CORNING MAGIC CORTISOL RADIOIMMUNO". The FDA issued a decision of Substantially Equivalent on September 4, 1984. The device falls under product code CGR (Radioimmunoassay, Cortisol), a Class II device regulated under 21 CFR 862.1205. Corning Medical & Scientific has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 4, 1984
Date Received
April 20, 1984
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