FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007

K Number: K083153 · Decision Feb 4, 2009
Classifications
1
FEI Numbers
242
Registration Numbers
243
Same Product Code
648
Applicant Total
85
Review Days
103

Basic Information

Device Name
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007
K Number
K083153
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
HOLLISTER, INC.
Date Received
October 24, 2008
Decision Date
February 4, 2009
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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