FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

BESMED VARIOUS MODELS OF TENS, BE-550/BE-660

K Number: K031374 · Decision Nov 28, 2003
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
10
Review Days
212

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Basic Information

Device Name
BESMED VARIOUS MODELS OF TENS, BE-550/BE-660
K Number
K031374
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Besmed Health Business Corp
Date Received
April 30, 2003
Decision Date
November 28, 2003
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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