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RP Lite 760R

FDA UDI

Class II (US FDA UDI)

by MEGO afek Agricultural Cooperative Society Ltd

Identity

Trade Name
RP Lite 760R FDA UDI
Generic Name
Sequential venous compression system inflator FDA UDI
Device Name
RP Lite® is a massage system intended for use by people in good health. As noted above, RP Lite® simulates the kneading and stroking action of manual massage by use of an inflatable garment that fills and deflates, applying a directional compress-and-release massage. This soothing massage action temporarily increases circulation in the areas to which the garment is applied, and temporarily relieves muscle aches and pain caused by fatigue or overexertion. FDA UDI
Model / Reference
760R FDA UDI
Description
RP Lite® is a massage system intended for use by people in good health. As noted above, RP Lite® simulates the kneading and stroking action of manual massage by use of an inflatable garment that fills and deflates, applying a directional compress-and-release massage. This soothing massage action temporarily increases circulation in the areas to which the garment is applied, and temporarily relieves muscle aches and pain caused by fatigue or overexertion. FDA UDI

Identifiers

Catalog Number
L10007AR FDA UDI
Primary DI / UDI-DI
07290105871497 FDA UDI
510(k) Number
K163280 FDA UDI
FDA Product Code
IRP FDA UDI
GMDN Term
Sequential venous compression system inflator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5650 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Sequential venous compression system inflator

RP Lite 760R by MEGO afek Agricultural Cooperative Society Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sequential venous compression system inflator.

Cleared under the same submission

K163280 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MEGO afek Agricultural Cooperative Society Ltd

Sources (1)

  • FDA UDI dcd836e3-4be7-4ef5-a853-33ac5f0fe3eb 36 fields · synced May 29, 2026