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

VIVONEX TUNGSTEN TIP TUBE-BRAIDED

K Number: K831968 · Decision Sep 1, 1983
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
10
Review Days
73

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Basic Information

Device Name
VIVONEX TUNGSTEN TIP TUBE-BRAIDED
K Number
K831968
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Norwich Eaton Pharmaceuticals, Inc.
Date Received
June 20, 1983
Decision Date
September 1, 1983
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)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNT), ordered by most recent decision date.

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Other Clearances by Norwich Eaton Pharmaceuticals, Inc.

K Number Device Name
K842841 VIVONEX TUNG STEN TIP TUBE
K831969 VIVONEX TUNGSTEN TIP TUBE-WOUND
K831971 VIVONEX TUNGSTEN TIP TUBE-TWISTED WIRE
K831970 VIVONEX TUNGSTEN TIP TUBE-MONOFILA-
K822516 VIVONEX MASS GASTRASTOMY TUBE
K821231 VIVONEX TUNGSTEN TIP TUBE PLACEMENT
K821067 VIVONEX ACUTROL ENTERNAL FEEDING SYS
K811968 VIVONEX TUNGSTEN TIP
K802300 VIVONEX JEJUNOSTOMY KIT