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

FENESTRATED INFUSION CATHETER

K Number: K024190 · Decision Mar 17, 2003
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
16
Review Days
88

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Basic Information

Device Name
FENESTRATED INFUSION CATHETER
K Number
K024190
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Promedic, Inc.
Date Received
December 19, 2002
Decision Date
March 17, 2003
Product Code
FRN
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
FRN Pump, Infusion

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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
K023579 GAS SAMPLING LINES
K020005 INFANT FEEDING TUBES
K970102 FILTER
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