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

MyOnyx System

K Number: K213197 · Decision Jun 17, 2022
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
22
Review Days
261

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Basic Information

Device Name
MyOnyx System
K Number
K213197
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Thought Technology , Ltd.
Date Received
September 29, 2021
Decision Date
June 17, 2022
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IPF), ordered by most recent decision date.

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Other Clearances by Thought Technology , Ltd.

K Number Device Name
K201014 MyOnyx System
K053434 MYOTRAC INFINITI ELECTRICAL STIMULATOR
K053266 MYOTRAC INFINITI
K925681 MYOTRAC2D/CS
K932149 THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE
K935213 INCONTROL
K915858 MYOTRAC2
K915859 MYOTRAC/S, MYODAC/S
K913898 MYOTRAC+/S, MYODAC+/S
K903497 FLEXCOMP DSP & PROCOMP
Search all 22 clearances from Thought Technology , Ltd. →