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

PEDIATRIC FEEDING TUBE

K Number: K052903 · Decision Nov 9, 2005
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
16
Review Days
26

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Basic Information

Device Name
PEDIATRIC FEEDING TUBE
K Number
K052903
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Promedic, Inc.
Date Received
October 14, 2005
Decision Date
November 9, 2005
Product Code
KNT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNT Tubes, Gastrointestinal (And Accessories)

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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
K031409 URINARY CATHETERS
K024190 FENESTRATED INFUSION CATHETER
K023579 GAS SAMPLING LINES
K020005 INFANT FEEDING TUBES
K970102 FILTER
Search all 16 clearances from Promedic, Inc. →