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

PICOSCALE BLOOD CELL COUNTER, MODEL PS-5

K Number: K860166 · Decision Apr 4, 1986
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
28
Review Days
77

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Basic Information

Device Name
PICOSCALE BLOOD CELL COUNTER, MODEL PS-5
K Number
K860166
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5200
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Diagnostic Technology, Inc.
Date Received
January 17, 1986
Decision Date
April 4, 1986
Product Code
GKL
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
GKL Counter, Cell, Automated (Particle Counter)

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K890819 HSV-CHECK(TM) TEST KIT
K871373 EBV-CHECK(TM) TEST KIT (IGG)
K864128 CHLAMYDIA-CHECK(TM) DIRECT & CULTURE CONFIR. KIT
K863408 EBV/VCA-CHECK(TM) ANTIGEN SLIDES
K860586 PHA-2 CONVERSION PROGRAM FOR PLATELET ANALYSIS
K853036 PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1
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