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

I.V. PRIMING SET

K Number: K913333 · Decision Oct 23, 1991
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
13
Review Days
89

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Basic Information

Device Name
I.V. PRIMING SET
K Number
K913333
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Gainor Medical Europe, Ltd.
Date Received
July 26, 1991
Decision Date
October 23, 1991
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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Other Clearances by Gainor Medical Europe, Ltd.

K Number Device Name
K926448 I.V. ADMINISTRATION SET
K931828 CARELET SAFETY LANCET
K931827 CLEANLET, CLEANLET XL & KIDS
K922441 SURESEAL BANDAGE
K902422 NEEDLE, ASPIRATION & INJECTION, DISPOSABLE
K902420 CATHETER, NASAL, OXYGEN
K902564 NEEDLE, DIALYSIS
K902426 HEMODIALYSIS SYSTEM AND ACCESSORY
K902421 STOMACH, GASTRO-ENTEROSTOMY
K902416 SURELITE AND SURELITE XL BLOOD LANCET
Search all 13 clearances from Gainor Medical Europe, Ltd. →