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

TM-400

K Number: K081247 · Decision Aug 25, 2008
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
70
Applicant Total
8
Review Days
116

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Basic Information

Device Name
TM-400
K Number
K081247
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5900
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ito Co., Ltd.
Date Received
May 1, 2008
Decision Date
August 25, 2008
Product Code
ITH
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
ITH Equipment, Traction, Powered

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Other Clearances by Ito Co., Ltd.

K Number Device Name
K203525 D function
K112520 US-101L, US-103S
K081943 MODEL ES-130
K032793 US-100 PORTABLE ULTRASOUND THERAPY UNIT
K022846 SW-180 SHORTWAVE THERAPY UNIT
K990787 TRIO 300
K992545 TM-300 TRACTION SYSTEM