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

QUANTIMETRIC PLUS CALIBRATOR/CONTROL SET A

K Number: K855014 · Decision Mar 14, 1986
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
301
Applicant Total
92
Review Days
88

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Basic Information

Device Name
QUANTIMETRIC PLUS CALIBRATOR/CONTROL SET A
K Number
K855014
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Kallestad Laboratories, Inc.
Date Received
December 16, 1985
Decision Date
March 14, 1986
Product Code
JIX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
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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Other Clearances by Kallestad Laboratories, Inc.

K Number Device Name
K863681 PATHFINDER(TM) DIRECT ANTIGEN DETECTION SYSTEM
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K863682 PATHFINDER(TM) SPECIMEN COLLECTION KIT
K862743 PATHFINDER(TM) RESPIRATORY SYNCYTIAL VIRUS
K862313 KALLESTAD SM/RNP TEST REAGENT
K862710 KALLESTAD SSA/SSB ENA TEST REAGENTS
K855010 QUANTIMETRIC PLUS IGM REAGENT KIT
K855009 QUANTIMETRIC PLUS IGA REAGENT KIT
K855008 QUANTIMETRIC PLUS KAPPA REAGENT KIT
K855013 QUANTIMETRIC PLUS SUPPORT PACK
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