FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

STM 9000 Basic, STM 9000 Standard, STM 9000 Fast, STM 9000 Ultra-Fast

K Number: K150220 · Decision Aug 19, 2015
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
13
Review Days
201

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Basic Information

Device Name
STM 9000 Basic, STM 9000 Standard, STM 9000 Fast, STM 9000 Ultra-Fast
K Number
K150220
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eb Neuro S.P.A.
Date Received
January 30, 2015
Decision Date
August 19, 2015
Product Code
GWF
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GWF Stimulator, Electrical, Evoked Response

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