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

CH-60 PLUS WHOLE BLOOD PLATELET CONTROL

K Number: K802141 · Decision Oct 10, 1980
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
191
Applicant Total
149
Review Days
35

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Basic Information

Device Name
CH-60 PLUS WHOLE BLOOD PLATELET CONTROL
K Number
K802141
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.8625
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
American Dade
Date Received
September 5, 1980
Decision Date
October 10, 1980
Product Code
JPK
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JPK Mixture, Hematology Quality Control

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K872789 PARAMAX URINE/CSF CALIBRATOR
K872195 DATA-FI DIMERTEST LATEX ASSAY
K872196 AQUEOUS BLOOD GAS/ELECTROLYTE CONTR LEV I,II & III
K871972 STRATUS IGE FLUOROMETRIC ENZYME IMMUNOASSAY
K871977 DADE MONI-TROL CHEMISTRY CONTROL/CALIBRATOR
K872050 PARAMAX CHOLESTEROL REAGENT
K872360 DATA-FI FIBRIN(OGEN) DEGRADATION PROD.(FDP)DET SET
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