FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇳 India

Torc Body

K Number: K192039 · Decision Mar 29, 2020
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
161
Applicant Total
3
Review Days
243

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Basic Information

Device Name
Torc Body
K Number
K192039
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Johari Digital Healthcare Limited
Date Received
July 30, 2019
Decision Date
March 29, 2020
Product Code
NGX
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
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

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