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

COULTER(R) MH010

K Number: K911385 · Decision Jun 17, 1991
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
379
Applicant Total
101
Review Days
81

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Basic Information

Device Name
COULTER(R) MH010
K Number
K911385
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Coulter Electronics, Inc.
Date Received
March 28, 1991
Decision Date
June 17, 1991
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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K922181 COULTER MH009
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K921567 COULTER MH017
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K905771 COULTER DART AST (GOT) REAGENT
K905767 COULTER DART ALT (GPT) REAGENT
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