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

GLUCOSE METER-CHECK SOLUTION FOR BAYER

K Number: K123966 · Decision Jan 25, 2013
Classifications
1
FEI Numbers
280
Registration Numbers
280
Same Product Code
492
Applicant Total
49
Review Days
30

Basic Information

Device Name
GLUCOSE METER-CHECK SOLUTION FOR BAYER
K Number
K123966
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BIONOSTICS, INC.
Date Received
December 26, 2012
Decision Date
January 25, 2013
Product Code
JJX
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

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