← Back to catalogue

Compressible Limb Therapy System(MK300L)

FDA UDI

Class II (US FDA UDI)

by Daesung Maref Co., Ltd.

Identity

Trade Name
Compressible Limb Therapy System(MK300L) FDA UDI
Generic Name
Pneumatic massager FDA UDI
Device Name
6 Chamber leg sleeve (Extra extra large) FDA UDI
Model / Reference
ACg0610-2 FDA UDI
Description
6 Chamber leg sleeve (Extra extra large) FDA UDI

Identifiers

Primary DI / UDI-DI
08809315679015 FDA UDI
510(k) Number
K112441 FDA UDI
FDA Product Code
IRP FDA UDI
GMDN Term
Pneumatic massager 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

Yes

FDA UDI

Over-the-Counter

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multi-chamber venous compression system garment, reusablePneumatic massager

Compressible Limb Therapy System(MK300L) by Daesung Maref Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pneumatic massager.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3815316b-ec80-4504-bba2-ed26d8d924a7 34 fields · synced Jun 8, 2026