510(k) K960246

LIQUID CARDIAC MARKER 1,2,3 ASSAYED by Ciba Corning Diagnostics Corp. — Product Code JJT

K960246 is an FDA 510(k) premarket notification submitted by Ciba Corning Diagnostics Corp. for the device "LIQUID CARDIAC MARKER 1,2,3 ASSAYED". The FDA issued a decision of Substantially Equivalent on April 23, 1996. The device falls under product code JJT (Enzyme Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Ciba Corning Diagnostics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 23, 1996
Date Received
January 16, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Controls (Assayed And Unassayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type