510(k) K820666

HUMAN C-PEPTIDE OF INSULIN BY RADIOIMM. by Immuno Nuclear Corp. — Product Code JKD

K820666 is an FDA 510(k) premarket notification submitted by Immuno Nuclear Corp. for the device "HUMAN C-PEPTIDE OF INSULIN BY RADIOIMM.". The FDA issued a decision of Substantially Equivalent on July 13, 1982. The device falls under product code JKD (Radioimmunoassay, C-Peptides Of Proinsulin), a Class I device regulated under 21 CFR 862.1135. Immuno Nuclear Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 13, 1982
Date Received
March 11, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, C-Peptides Of Proinsulin
Device Class
Class I
Regulation Number
862.1135
Review Panel
CH
Submission Type