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

TRIO 300

K Number: K990787 · Decision Oct 20, 1999
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
8
Review Days
224

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Basic Information

Device Name
TRIO 300
K Number
K990787
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ito Co., Ltd.
Date Received
March 10, 1999
Decision Date
October 20, 1999
Product Code
IPF
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
IPF Stimulator, Muscle, Powered

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K Number Device Name
K203525 D function
K112520 US-101L, US-103S
K081943 MODEL ES-130
K081247 TM-400
K032793 US-100 PORTABLE ULTRASOUND THERAPY UNIT
K022846 SW-180 SHORTWAVE THERAPY UNIT
K992545 TM-300 TRACTION SYSTEM