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

Chattanooga Revolution Wireless

K Number: K153696 · Decision Apr 14, 2016
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
543
Applicant Total
12
Review Days
113

Basic Information

Device Name
Chattanooga Revolution Wireless
K Number
K153696
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DJO, LLC
Date Received
December 23, 2015
Decision Date
April 14, 2016
Product Code
IPF
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IPF Stimulator, Muscle, Powered

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