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

PAJUNK MULTISTIM SENSOR NERVE STIMULATORS

K Number: K061172 · Decision Oct 17, 2006
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
62
Applicant Total
44
Review Days
173

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Basic Information

Device Name
PAJUNK MULTISTIM SENSOR NERVE STIMULATORS
K Number
K061172
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2775
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PAJUNK GmbH Medizintechnologie
Date Received
April 27, 2006
Decision Date
October 17, 2006
Product Code
BXN
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
BXN Stimulator, Nerve, Battery-Powered

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