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

PAJUNK STANDARD SPROTTE NEEDLE W/ INTRODUCER CANN.

K Number: K923003 · Decision Apr 15, 1993
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
151
Applicant Total
26
Review Days
297

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Basic Information

Device Name
PAJUNK STANDARD SPROTTE NEEDLE W/ INTRODUCER CANN.
K Number
K923003
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Rusch, Inc.
Date Received
June 22, 1992
Decision Date
April 15, 1993
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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