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

SYSMEX SE/RAM-1

K Number: K964375 · Decision Mar 13, 1997
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
18
Review Days
132

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Basic Information

Device Name
SYSMEX SE/RAM-1
K Number
K964375
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5200
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sysmex Corp.
Date Received
November 1, 1996
Decision Date
March 13, 1997
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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Other Clearances by Sysmex Corp.

K Number Device Name
K012372 SYSMEX UF-50
K992875 SYSMEX XE-2100, AUTOMATATED HEMATOLOGY ANALYZER
K981950 SYSMEX R-3500, AUTOMATED RETICCULOCYTE ANALYZER, MODEL R-3500
K981761 SYSMEX KX-21, AUTOMATED HEMATOLOGY ANALYZER
K971736 SYSMEX IMMATURE RETICULOCYTE FRACTION (IRF) PARAMETER
K964946 SYSMEX CA-1000/SYSMEX CA-5000
K961054 SYSMEX UF-100
K950508 SYSMEX SF-3000
K945837 SYSMEX(TM) F-820, 520
K942097 TOA MEDICAL ELECTRONICS CA-5000
Search all 18 clearances from Sysmex Corp. →