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

PAB IV CONTAINER

K Number: K840388 · Decision Mar 6, 1984
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
13
Review Days
36

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Basic Information

Device Name
PAB IV CONTAINER
K Number
K840388
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
American Mcgaw
Date Received
January 30, 1984
Decision Date
March 6, 1984
Product Code
KPE
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
KPE Container, I.V.

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K840212 CONCENTRATED PLATELET ADMIN. SET
K831716 CAPD - CATHETER ADAPTER
K822240 ETHYLENE OXIDE STERILIZ. PARAMETRIC REL.
K820133 MCGAW FAT EMULSION SET
K813092 ACCUPRO I.V. ADMINISTRATION SET
K810683 CAPD CATHETER ADAPTER
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