510(k) K990434

CARESIDE CKMB by Careside, Inc. — Product Code JHS

K990434 is an FDA 510(k) premarket notification submitted by Careside, Inc. for the device "CARESIDE CKMB". The FDA issued a decision of Substantially Equivalent on April 19, 1999. The device falls under product code JHS (Differential Rate Kinetic Method, Cpk Or Isoenzymes), a Class II device regulated under 21 CFR 862.1215. Careside, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 19, 1999
Date Received
February 11, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Differential Rate Kinetic Method, Cpk Or Isoenzymes
Device Class
Class II
Regulation Number
862.1215
Review Panel
CH
Submission Type