FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Air Compression Leg Massager (UM605, UM606, UM607, UM608,UM609,UM610, UM611, UM617)

K Number: K250046 · Decision Apr 25, 2025
Classifications
1
FEI Numbers
95
Registration Numbers
95
Same Product Code
152
Applicant Total
8
Review Days
105

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Basic Information

Device Name
Air Compression Leg Massager (UM605, UM606, UM607, UM608,UM609,UM610, UM611, UM617)
K Number
K250046
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5650
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shenzhen Urion Technology Co., Ltd.
Date Received
January 10, 2025
Decision Date
April 25, 2025
Product Code
IRP
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
IRP Massager, Powered Inflatable Tube

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K241007 Upper Arm Electronic Blood Pressure Monitor (U86E and TelliBP01)
K200802 Infrared Thermometer
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K141683 ELECTRONIC BLOOD PRESSURE MONITOR