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

ALARA Neuro Access Kit

K Number: K190163 · Decision Jul 16, 2019
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
34
Applicant Total
25
Review Days
166

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Basic Information

Device Name
ALARA Neuro Access Kit
K Number
K190163
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1820
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SurGenTec, LLC
Date Received
January 31, 2019
Decision Date
July 16, 2019
Product Code
PDQ
Advisory Committee
Ear, Nose, Throat
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
PDQ Neurosurgical Nerve Locator

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K242797 OsteoFlo HydroFiber
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