FDA UDI Not in Commercial Distribution 🇺🇸 United States

LiteWalk

DI: 07290016880250 · Model: LiteWalk · VIASONIX LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LiteWalk
Primary DI
07290016880250
Version / Model
LiteWalk
Company Name
VIASONIX LTD
Labeler DUNS
533070236
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-19
Public Version
1
Public Version Date
2020-06-29
Public Version Status
New
Public Device Record Key
33ce01c7-d3d1-433a-af5a-b4be693d4a98
Distribution End Date
2020-06-19

Device Description

The LiteWalk is Intended for home and hospital use for temporary increase in local blood circulation in the lower extremities and temporary relief of minor muscle aches and pains where applied. The system is based on a pneumatic unit that includes a pump, valves, pressure sensor and tubing, and is fed by an external power supply of 12V DC. The LiteWalk doesn't contains a software user interface. The 2 sandals (right/left) are inflated together at the same time with the same pump. The inflation cycle is sequential, as follows: inflate heel, inflate arch, deflate heel, inflate metatarsals, deflate arch, inflate toes, deflate metatarsals, deflate toes

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IRP Massager, Powered Inflatable Tube

GMDN Terms

Code Name
16837 Sequential venous compression system

Identifiers

Type ID
Primary 07290016880250

Premarket Submissions

Submission Number Supplement Number
K192607 000