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

ISOFLUX IXZ FLOW REGULATOR

K Number: K925732 · Decision May 9, 1994
Classifications
1
FEI Numbers
437
Registration Numbers
437
Same Product Code
1167
Applicant Total
57
Review Days
542

Basic Information

Device Name
ISOFLUX IXZ FLOW REGULATOR
K Number
K925732
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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