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

US-100 PORTABLE ULTRASOUND THERAPY UNIT

K Number: K032793 · Decision Oct 9, 2003
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
88
Applicant Total
8
Review Days
30

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Basic Information

Device Name
US-100 PORTABLE ULTRASOUND THERAPY UNIT
K Number
K032793
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5300
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ito Co., Ltd.
Date Received
September 9, 2003
Decision Date
October 9, 2003
Product Code
IMI
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
IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

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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
K081247 TM-400
K022846 SW-180 SHORTWAVE THERAPY UNIT
K990787 TRIO 300
K992545 TM-300 TRACTION SYSTEM