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

VYGON SPLIT CANNULA INTRODUCER

K Number: K010913 · Decision Sep 28, 2001
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
48
Review Days
185

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Basic Information

Device Name
VYGON SPLIT CANNULA INTRODUCER
K Number
K010913
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vygon Corp.
Date Received
March 27, 2001
Decision Date
September 28, 2001
Product Code
DYB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DYB Introducer, Catheter

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Other Clearances by Vygon Corp.

K Number Device Name
K121105 NUTRISAFE 2 FEEDING TUBE
K100163 NUTRISAFE 2 FEEDING TUBES MODEL 362.XXX. 1362.XXX
K073493 HEPATOSTAT SET
K070705 MODIFICATION TO: LATEX-FREE BIONECTOR, MODEL# 896.019, 896.039
K061796 HEPATOSTAT SET, MODEL 760X
K061250 MULTICATH EXPERT
K060944 NUTRISAFE 2
K062425 LIFECATH S PICC AND MIDLINE CATHETER
K052564 VYGON LEADER-FLEX
K052881 VYGON LATEX FREE BIONECTOR
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