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

PHARMAFEED

K Number: K932649 · Decision Nov 16, 1993
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
16
Review Days
167

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Basic Information

Device Name
PHARMAFEED
K Number
K932649
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Plasco, Inc.
Date Received
June 2, 1993
Decision Date
November 16, 1993
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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K950770 CPR MICROSHIELD II
K943386 CPR MICROMASK
K880337 MACBICK DISPOSABLE BARIUM ENEMA SYST 4800 & 4700
K870623 ENTERAL ADMINISTRATION SET
K870019 THE LAHR BALLOON
K870796 MACBICK-XL BASIC AIR CONTAST BARIUM ENEMA DELIV SY
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