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

BIONAVIGATION SYSTEM FOR PLACEMENT OF ENTERAL FEEDING TUBES

K Number: K983476 · Decision Mar 1, 1999
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
5
Review Days
150

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Basic Information

Device Name
BIONAVIGATION SYSTEM FOR PLACEMENT OF ENTERAL FEEDING TUBES
K Number
K983476
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Navion Biomedical Corp.
Date Received
October 2, 1998
Decision Date
March 1, 1999
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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K940385 NAVIGATOR-MP CATHETER LOCATION INSTRUMENT
K901263 NAVION SMART-WIRE(TM) CATHETER LOCATION SYSTEM