510(k) K821374

ENZYMUNE-TEST INSULIN by Icl Scientific — Product Code CFP

K821374 is an FDA 510(k) premarket notification submitted by Icl Scientific for the device "ENZYMUNE-TEST INSULIN". The FDA issued a decision of Substantially Equivalent on May 28, 1982. The device falls under product code CFP (Radioimmunoassay, Immunoreactive Insulin), a Class I device regulated under 21 CFR 862.1405. Icl Scientific has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 28, 1982
Date Received
May 10, 1982
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