510(k) K062751

MODIFICATION TO QUANTIMETRIX CARDIASURE CARDIAC MARKER by Quantimetrix Corp. — Product Code JJT

K062751 is an FDA 510(k) premarket notification submitted by Quantimetrix Corp. for the device "MODIFICATION TO QUANTIMETRIX CARDIASURE CARDIAC MARKER". The FDA issued a decision of Substantially Equivalent on October 3, 2006. The device falls under product code JJT (Enzyme Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Quantimetrix Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 3, 2006
Date Received
September 14, 2006
Clearance Type
Special
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