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

IV ADMINISTRATION SET WITH BACKCHECK

K Number: K790062 · Decision Apr 10, 1979
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
34
Review Days
90

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Basic Information

Device Name
IV ADMINISTRATION SET WITH BACKCHECK
K Number
K790062
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
National Patent Development Corp.
Date Received
January 10, 1979
Decision Date
April 10, 1979
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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