510(k) K944243

CARDIOCHEX by Cala Diagnostics — Product Code JJT

K944243 is an FDA 510(k) premarket notification submitted by Cala Diagnostics for the device "CARDIOCHEX". The FDA issued a decision of Substantially Equivalent on October 27, 1994. The device falls under product code JJT (Enzyme Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Cala Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 27, 1994
Date Received
August 31, 1994
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