510(k) K896420

DSL C-PEPTIDE RIA (DSL #7000) by Diagnostic Systems Laboratories, Inc. — Product Code JKD

K896420 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "DSL C-PEPTIDE RIA (DSL #7000)". The FDA issued a decision of Substantially Equivalent on May 24, 1990. The device falls under product code JKD (Radioimmunoassay, C-Peptides Of Proinsulin), a Class I device regulated under 21 CFR 862.1135. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 24, 1990
Date Received
November 8, 1989
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