FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PRECISET SERUM PROTEINS CALIBRATOR

K Number: K983469 · Decision Nov 25, 1998
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
301
Applicant Total
340
Review Days
55

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Basic Information

Device Name
PRECISET SERUM PROTEINS CALIBRATOR
K Number
K983469
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Boehringer Mannheim Corp.
Date Received
October 1, 1998
Decision Date
November 25, 1998
Product Code
JIX
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
JIX Calibrator, Multi-Analyte Mixture

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K Number Device Name
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K984425 MODIFICATION OF PRECISET SERUM PROTEINS CALIBRATOR
K984372 ELECSYS CALCHECK TROPONIN T
K984105 ELECSYS TROPONIN T STAT TEST
K983503 ROCHE DIAGNOSTICS, BOEHRINGER MANNHEIM CORPORATION INORGANIC PHOSPHORUS REAGENT CATALOG NUMBER 1730347
K983185 BOEHRINGER MANNHEIM TINA-QUANT IGE TEST
K982949 ELECSYS PSA, MODEL 2010
K982948 ELECSYS PSA, MODEL # ELECSYS 1010
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