510(k) K874087

MODIFIED CALCITONIN RIA KIT DSL #1200 by Diagnostic Systems Laboratories, Inc. — Product Code JKR

K874087 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "MODIFIED CALCITONIN RIA KIT DSL #1200". The FDA issued a decision of Substantially Equivalent on February 2, 1988. The device falls under product code JKR (Radioimmunoassay, Calcitonin), a Class II device regulated under 21 CFR 862.1140. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 2, 1988
Date Received
October 7, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Calcitonin
Device Class
Class II
Regulation Number
862.1140
Review Panel
CH
Submission Type