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

WHOLE BLOOD GLUCOSE CONTROL LEVEL 1,2,AND 3/WHOLE BLOOD GLUCOSE LINEARITY CONTROL-LEVEL1,2,3,4,5,AND 6

K Number: K964278 · Decision Nov 22, 1996
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
17
Review Days
25

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Basic Information

Device Name
WHOLE BLOOD GLUCOSE CONTROL LEVEL 1,2,AND 3/WHOLE BLOOD GLUCOSE LINEARITY CONTROL-LEVEL1,2,3,4,5,AND 6
K Number
K964278
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Clinical Controls, Inc.
Date Received
October 28, 1996
Decision Date
November 22, 1996
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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K946265 FIBRINOGEN HIGH ABNORMAL CONTROL - LEVEL 3
K935598 PLASMA FIBRINOGEN CONTROL LEVEL 1/LEVEL 2
K946049 LIQUISPEX(TM) LIQUID B2M/CRP CONTROL LEVEL 1 AND 2
K946048 LIQUISPEX(TM) LIQUID B2M CONTROL LEVEL 1 AND 2
K946050 LIQUISPEX(TM) LIQUID CRP CONTROL LEVEL 1 AND 2
K946266 FERRITIN CONTROL - LEVEL 1, 2, 3
K946144 LIQUISPEX(TM) URINE ETHANOL CONTROL
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