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

INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA)

K Number: K952160 · Decision Sep 21, 1995
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
48
Review Days
136

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Basic Information

Device Name
INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA)
K Number
K952160
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medex, Inc.
Date Received
May 8, 1995
Decision Date
September 21, 1995
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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