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

HEMACHECK

K Number: K781562 · Decision Nov 15, 1978
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
22
Review Days
65

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Basic Information

Device Name
HEMACHECK
K Number
K781562
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5200
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Vickers America Medical Corp.
Date Received
September 11, 1978
Decision Date
November 15, 1978
Product Code
GKL
Advisory Committee
Hematology
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
GKL Counter, Cell, Automated (Particle Counter)

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K830936 TREONIC IP5
K813239 OXYGENAIRE NURING INCUBATOR
K813238 NEOCARE BABY-CONTROLLED INCUBATOR
K811865 VMA PEDIATRIC APNEA MATTRESS
K810792 NEOCARE TEMPERATURE MONITOR
K810067 140 NEOCARE AIR CONTROLLED INCUBATOR
K810571 NEOCARE OXYGEN MONITOR
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