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

CARDIAC MARKERS CONTROL (SINGLE USE)-LEVELS, 1,2,3, MODELS NUMBER 175-1, 175-2, 175-3

K Number: K982845 · Decision Aug 21, 1998
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
96
Applicant Total
16
Review Days
9

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Basic Information

Device Name
CARDIAC MARKERS CONTROL (SINGLE USE)-LEVELS, 1,2,3, MODELS NUMBER 175-1, 175-2, 175-3
K Number
K982845
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
More Diagnostics
Date Received
August 12, 1998
Decision Date
August 21, 1998
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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