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

Wireless Audio System

K Number: K173409 · Decision Feb 16, 2018
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
17
Review Days
107

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Basic Information

Device Name
Wireless Audio System
K Number
K173409
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neocoil, LLC
Date Received
November 1, 2017
Decision Date
February 16, 2018
Product Code
LNH
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LNH System, Nuclear Magnetic Resonance Imaging

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