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

VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193

K Number: K851479 · Decision Jun 14, 1985
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
48
Review Days
60

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Basic Information

Device Name
VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193
K Number
K851479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5140
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Vygon Corp.
Date Received
April 15, 1985
Decision Date
June 14, 1985
Product Code
CAZ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CAZ Anesthesia Conduction Kit

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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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