FDA 510(k) FDA class 2 Substantially Equivalent 🇭🇰 Hong Kong

MEDISANA DIGITAL TENS

K Number: K994265 · Decision Jul 6, 2000
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
7
Review Days
202

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Basic Information

Device Name
MEDISANA DIGITAL TENS
K Number
K994265
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Fuji Dynamics Limited
Date Received
December 17, 1999
Decision Date
July 6, 2000
Product Code
GZJ
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
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

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Other Clearances by Fuji Dynamics Limited

K Number Device Name
K092780 INF 4160 PLUS, MODEL D-FJ31F
K063642 FD EMS, MODEL # D-FJ30E
K052813 FD TENS 2030, MODEL DFJ24T
K043407 INF 4160, MODEL D-FJ27F
K041164 L-TENS
K994266 FDTENS 2010