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

ISOFLUX IXP FLOW REGULATOR

K Number: K925731 · Decision May 9, 1994
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
57
Review Days
542

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Basic Information

Device Name
ISOFLUX IXP FLOW REGULATOR
K Number
K925731
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ferguson Medical
Date Received
November 13, 1992
Decision Date
May 9, 1994
Product Code
FPA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FPA Set, Administration, Intravascular

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