FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3

K Number: K925151 · Decision Dec 17, 1992
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
96
Applicant Total
319
Review Days
65

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Basic Information

Device Name
LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3
K Number
K925151
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bio-Rad
Date Received
October 13, 1992
Decision Date
December 17, 1992
Product Code
JJT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JJT Enzyme Controls (Assayed And Unassayed)

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