FDA 510(k) Unknown 🇺🇸 United States

FREKATHETER VENOUS CATHETERISATION SYS

K Number: K841718 · Decision Apr 25, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
38
Review Days

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Basic Information

Device Name
FREKATHETER VENOUS CATHETERISATION SYS
K Number
K841718
Clearance Type
Traditional
Decision
Unknown
Applicant
Fresenius USA, Inc.
Date Received
April 25, 1984
Decision Date
April 25, 1984
Advisory Committee
Unknown
Review Advisory Committee
CV
Third Party
N

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