510(k) K833396

C-PEPTIDE RADIOIMMUNOASSAY TEST KIT by Serono Diagnostics, Inc. — Product Code JKD

K833396 is an FDA 510(k) premarket notification submitted by Serono Diagnostics, Inc. for the device "C-PEPTIDE RADIOIMMUNOASSAY TEST KIT". The FDA issued a decision of Substantially Equivalent on April 13, 1984. The device falls under product code JKD (Radioimmunoassay, C-Peptides Of Proinsulin), a Class I device regulated under 21 CFR 862.1135. Serono Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 13, 1984
Date Received
September 30, 1983
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