FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

MultiStim ECO

K Number: K162086 · Decision Jan 6, 2017
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
62
Applicant Total
44
Review Days
163

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Basic Information

Device Name
MultiStim ECO
K Number
K162086
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
July 27, 2016
Decision Date
January 6, 2017
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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K230201 Disposable Pre-calibrated Brain Biopsy Needle 2.0
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