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

IV SET WITH GRADUATED CHAMBER

K Number: K781744 · Decision Dec 7, 1978
Classifications
1
FEI Numbers
437
Registration Numbers
437
Same Product Code
1167
Applicant Total
34
Review Days
48

Basic Information

Device Name
IV SET WITH GRADUATED CHAMBER
K Number
K781744
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
October 20, 1978
Decision Date
December 7, 1978
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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