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

VYGON SPINAL ANESTHESIA NEEDLE W/INTRODUCER 183

K Number: K851478 · Decision May 7, 1985
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
151
Applicant Total
48
Review Days
22

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Basic Information

Device Name
VYGON SPINAL ANESTHESIA NEEDLE W/INTRODUCER 183
K Number
K851478
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Vygon Corp.
Date Received
April 15, 1985
Decision Date
May 7, 1985
Product Code
BSP
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
BSP Needle, Conduction, Anesthetic (W/Wo Introducer)

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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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