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

NomadAir PMU810

K Number: K220631 · Decision Jul 15, 2022
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
52
Applicant Total
9
Review Days
133

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Basic Information

Device Name
NomadAir PMU810
K Number
K220631
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1835
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neurotronics, Inc.
Date Received
March 4, 2022
Decision Date
July 15, 2022
Product Code
GWL
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
GWL Amplifier, Physiological Signal

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