FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

PROTEKTOR 32

K Number: K093304 · Decision Aug 11, 2010
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
12
Review Days
294

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Basic Information

Device Name
PROTEKTOR 32
K Number
K093304
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Natus Medical, Inc.
Date Received
October 21, 2009
Decision Date
August 11, 2010
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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