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

QUANTIMETRIC C-REACTIVE PROTEIN ASSAY R.

K Number: K811617 · Decision Jun 25, 1981
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
92
Review Days
17

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Basic Information

Device Name
QUANTIMETRIC C-REACTIVE PROTEIN ASSAY R.
K Number
K811617
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Kallestad Laboratories, Inc.
Date Received
June 8, 1981
Decision Date
June 25, 1981
Product Code
DCK
Advisory Committee
Immunology
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
DCK C-Reactive Protein, Antigen, Antiserum, And Control

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Other Clearances by Kallestad Laboratories, Inc.

K Number Device Name
K863681 PATHFINDER(TM) DIRECT ANTIGEN DETECTION SYSTEM
K862917 PATHFINDER ROTAVIRUS CHEMILUMINESCENT
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
K855014 QUANTIMETRIC PLUS CALIBRATOR/CONTROL SET A
K855010 QUANTIMETRIC PLUS IGM REAGENT KIT
K855009 QUANTIMETRIC PLUS IGA REAGENT KIT
K855008 QUANTIMETRIC PLUS KAPPA REAGENT KIT
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