510(k) K812227

GAMMACOAT (125) INSULIN RADIOIMMUNOASSAY by Clinical Assays, Inc. — Product Code CFP

K812227 is an FDA 510(k) premarket notification submitted by Clinical Assays, Inc. for the device "GAMMACOAT (125) INSULIN RADIOIMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on September 24, 1981. The device falls under product code CFP (Radioimmunoassay, Immunoreactive Insulin), a Class I device regulated under 21 CFR 862.1405. Clinical Assays, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 24, 1981
Date Received
August 10, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Immunoreactive Insulin
Device Class
Class I
Regulation Number
862.1405
Review Panel
CH
Submission Type