FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VYGON CANNULA FOR SURGICAL SUCTION YAN KAUER 574/5

K Number: K851475 · Decision May 3, 1985
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
48
Review Days
18

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Basic Information

Device Name
VYGON CANNULA FOR SURGICAL SUCTION YAN KAUER 574/5
K Number
K851475
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Vygon Corp.
Date Received
April 15, 1985
Decision Date
May 3, 1985
Product Code
GBX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GBX Catheter, Irrigation

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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
Search all 48 clearances from Vygon Corp. →