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

LIQUID IMMUNOLOGY CONTROL LEVEL I, II, III

K Number: K963085 · Decision Aug 20, 1996
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
7
Review Days
12

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Basic Information

Device Name
LIQUID IMMUNOLOGY CONTROL LEVEL I, II, III
K Number
K963085
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
International Enzymes, Inc.
Date Received
August 8, 1996
Decision Date
August 20, 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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K Number Device Name
K011169 HSCRP CONTROL LEVEL 1, HSCRP CONTROL LEVEL 2, AND HSCRP CONTROL LEVEL 3
K953927 LINICAL PROTEIN VI CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN ARRAY PROTEIN SYSTEM
K953926 LINICAL PROTEIN III CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN ARRAY PROTEIN SYSTEM
K950802 LINICAL PROTEIN I CALIBRATION VERIFIERS LEVELS A - FOR BECKMAN ARRAY 360 SYSTEM
K944486 LINICAL PROTEIN I CALIBRATION VERIFIERS LEVELS A - E
K944513 LINICAL PROTEIN VI CALIBRATION VERIFIERS LEVELS A-E