FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PRESSURIZER

K Number: K951988 · Decision Jun 14, 1995
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
34
Applicant Total
16
Review Days
48

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Basic Information

Device Name
PRESSURIZER
K Number
K951988
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5420
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Promedic, Inc.
Date Received
April 27, 1995
Decision Date
June 14, 1995
Product Code
KZD
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
KZD Infusor, Pressure, For I.V. Bags

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Other Clearances by Promedic, Inc.

K Number Device Name
K131889 EUM 100PRO
K112318 CLEARPATH 24
K072756 NON-IV ADAPTER FOR INFANT NG TUBE
K060497 BABYAIR
K060842 REVJET TURBO
K052903 PEDIATRIC FEEDING TUBE
K031409 URINARY CATHETERS
K024190 FENESTRATED INFUSION CATHETER
K023579 GAS SAMPLING LINES
K020005 INFANT FEEDING TUBES
Search all 16 clearances from Promedic, Inc. →