510(k) K914429

DSL ULTRA-SENSITIVE CALCITONIN RIA (DSL 5200) by Diagnostic Systems Laboratories, Inc. — Product Code JKR

K914429 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "DSL ULTRA-SENSITIVE CALCITONIN RIA (DSL 5200)". The FDA issued a decision of Substantially Equivalent on January 15, 1992. 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
January 15, 1992
Date Received
October 4, 1991
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