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

ROCHE COBAS MICROS HEMATOLOGY ANALYZER

K Number: K953448 · Decision Oct 13, 1995
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
379
Applicant Total
296
Review Days
88

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Basic Information

Device Name
ROCHE COBAS MICROS HEMATOLOGY ANALYZER
K Number
K953448
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Roche Diagnostic Systems, Inc.
Date Received
July 17, 1995
Decision Date
October 13, 1995
Product Code
GKZ
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
GKZ Counter, Differential Cell

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K983556 ABUSCREEN ONLINE BENZ 300 CALIBRATORS
K983555 ABUSCREEN ONLINE BENZ 200 CALIBRATORS
K983697 MODIFICATION TO ABUSCREEN ONLINE COCAINE METABOLITE
K983700 MODIFICATION TO ABUSCREEN ONLINE FOR PROPOXYPHENE
K983701 MODIFICATION TO ABUSCREEN ONLINE FOR CANNABINOIDS
K983699 MODIFICATION TO ABUSCREEN ONLINE FOR AMPHETAMINES
K983703 MODIFICATION TO ABUSCREEN ONLINE FOR METHADONE
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