510(k) K872063

TANDEM-E IMMUNOENZYMETRIC ASSAY FOR CKMB II by Hybritech, Inc. — Product Code JHY

K872063 is an FDA 510(k) premarket notification submitted by Hybritech, Inc. for the device "TANDEM-E IMMUNOENZYMETRIC ASSAY FOR CKMB II". The FDA issued a decision of Substantially Equivalent on June 19, 1987. The device falls under product code JHY (Colorimetric Method, Cpk Or Isoenzymes), a Class II device regulated under 21 CFR 862.1215. Hybritech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 19, 1987
Date Received
May 28, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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