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

AQUEOUS ETHANOL/AMMONIA CONTROL LEVEL 1, 2, & 3

K Number: K955690 · Decision Apr 24, 1996
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
17
Review Days
132

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Basic Information

Device Name
AQUEOUS ETHANOL/AMMONIA CONTROL LEVEL 1, 2, & 3
K Number
K955690
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
December 14, 1995
Decision Date
April 24, 1996
Product Code
JJY
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
JJY Multi-Analyte Controls, All Kinds (Assayed)

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Other Clearances by Clinical Controls, Inc.

K Number Device Name
K964278 WHOLE BLOOD GLUCOSE CONTROL LEVEL 1,2,AND 3/WHOLE BLOOD GLUCOSE LINEARITY CONTROL-LEVEL1,2,3,4,5,AND 6
K962432 LIQUISPEX URINE (MICRO)ALBUMIN CONTROL
K955691 SERUM VOLATILES CONTROL LEVEL 1 & 2
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
Search all 17 clearances from Clinical Controls, Inc. →