510(k) K854066

DOUBLE ANTIBODY C-PEPTIDE RIA KIT by Diagnostic Products Corp. — Product Code JKD

K854066 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "DOUBLE ANTIBODY C-PEPTIDE RIA KIT". The FDA issued a decision of Substantially Equivalent on November 12, 1985. The device falls under product code JKD (Radioimmunoassay, C-Peptides Of Proinsulin), a Class I device regulated under 21 CFR 862.1135. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 12, 1985
Date Received
October 4, 1985
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