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

DIFFERENTIAL COUNTING BOARD

K Number: K915071 · Decision Jan 17, 1992
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
379
Applicant Total
11
Review Days
70

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Basic Information

Device Name
DIFFERENTIAL COUNTING BOARD
K Number
K915071
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Biovation, Inc.
Date Received
November 8, 1991
Decision Date
January 17, 1992
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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Other Clearances by Biovation, Inc.

K Number Device Name
K925528 BIOVATION K-MANAGER
K923844 LYRIS 100/120 LABORATORY INFORMATION SYSTEM
K853026 BIOVATION MAX DATA MANAGEMENT SYSTEM
K842401 CHEMISTRY CONSOLE
K831830 LYRIS MODULAR INFO SYSTEM
K821534 HEMATOLOGY DATA MANAGEMENT SYS
K812604 BIOVATION URINALYSIS REPORTER
K792045 BIOVATION NEPHELOMETER
K790862 BIOVATION DIGITAL URINOMETER
K781644 ANTIBIOTIC NEPHELOMETER
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