COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008

K102319 · Won Industrial Co. · IRP · Jan 28, 2011 · Physical Medicine

Device Facts

• Record ID: K102319
• Device Name: COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008
• Applicant: Won Industrial Co.
• Product Code: IRP · Physical Medicine
• Decision Date: Jan 28, 2011
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 890.5650
• Device Class: Class 2
• Attributes: Therapeutic

Indications for Use

WIC-2008 is intended for use by medical professionals and patients at home, who are under medical supervision, in treating many conditions, such as : Primary lymphedema, Edema following trauma and sport injuries, Postimmobilization edema, Venous insufficiencies, Lymphedema.

Device Story

WIC-2008 is a powered inflatable tube massager used for compressible limb therapy. The system utilizes four-chamber garments applied to the leg. The power unit controls variable duration, pressure, cycle time, and gradient settings to provide pneumatic compression. It features visual status and fault indicators. Used in clinical or home settings under medical supervision to manage edema and venous conditions. The device assists in fluid mobilization, potentially reducing swelling and improving circulation for patients with lymphedema or post-traumatic edema.

Clinical Evidence

Bench testing only. No clinical data provided.

Technological Characteristics

Powered inflatable tube massager; four-chamber garment system. Features variable pressure, cycle time, and gradient settings. Electrical safety per IEC 60601-1, IEC 60601-2-10, and IEC 60601-1-2. Quality management per ISO 13485:2003. Risk management per ISO 14971:2007.

Indications for Use

Indicated for patients requiring treatment for primary lymphedema, edema following trauma/sports injuries, post-immobilization edema, venous insufficiencies, and lymphedema. Intended for use by medical professionals or patients at home under medical supervision.

Regulatory Classification

Identification

A powered inflatable tube massager is a powered device intended for medical purposes, such as to relieve minor muscle aches and pains and to increase circulation. It simulates kneading and stroking of tissues with the hands by use of an inflatable pressure cuff.

Predicate Devices

• Compressible Limb and Circulation Therapy Systems (WHF-324 (POWER-Q1000 PLUS)) (K100656)

Submission Summary (Full Text)

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# K102319

Page 1 of 2

# 510(K) SUMMARY

[as required by 807.92(c)]

JAN 2 8 2011

## A. 510k Number:

#### B. Applicant:

Company name: PATS CORP Address: 49 Candlewood Way, Buena Park, CA 90621, USA Contact person: Mr Brandon Choi Phone: [phone] Fax: [phone]

C. Proprietary and Established Names: WON INDUSTRY CO LTD

Address: 22-5,Daeya-dong,Siheung-si,Gyeonggi-do, Korea

## D. Regulatory Information

- 1. Classification Name: Massager, Powered Inflatable Tube
- 2. Common / Usual Name: Powered Inflatable Tube Massager
- 3. Proprietary Name: Compressible Limb Therapy System WIC-2008
- 4. Classification / Product Code: Class II / IRP (21 CFR 890.5650)

#### E. Intended Use

WIC-2008 is intended for use by medical professionals and patients at home, who are under medical supervision, in treating many conditions, such as : Primary lymphedema, Edema following trauma and sport injuries, Postimmobilization edema, Venous insufficiencies, Lymphedema.

# F. Device Description

WIC-2008 is used with four chamber garments for full leg, and period has its own variable duration,pressure, cycle time and gradient setting. Power unit features visual operation statusand fault indicators.

#### G. Substantial Equivalence Information

Predicate Device

- Classification: 2
- 510(k) number: K100656
- Name: Compressible Limb and Circulation Therapy Systems

(WHF-324 (POWER-Q1000 PLUS))

#### 1. Comparison with predicate

Compressible Limb Therapy System WIC-2008 has substantial equivalent intended use as the-market-cleared WHF-324 (POWER-Q1000 PLUS) and has substantial equivalent technological and performance characteristics. After analyzing both bench as well as laboratory testing to applicable standards,

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it is the conclusion of WON INDUSTRY Co Ltd. that Compressible Limb Therapy System WIC-2008 is as safe and effective as the predicate devices, has few technological differences, but there are no new indications for use and without raising any new safety and/or effectiveness concerns. Concerns. Concerns it is clear that it substantially equivalent to the predicate devices

102319

page 2 of 2

# H. Performance Characteristics (If/when applicable)

WIC-2008has conducted and applied by standard of

- Council Directive 93/42/EEC of 14 June 1993 concerning medical devices .
- IEC 980:2003, Graphical symbols for use in the labeling of medical devices .
- IEC1041:1998, Information supplied by the manufacturer with medical devices .
- ISO 13485:2003, Medical devices Quality management systems -. Requirements for regulatory purposes
- ISO 14155-1:2003, Clinical investigation of medical devices for human subjects . - Part 1: General requirements
- ISO 14971:2007, Medical devices Application of risk management to medical devices
- IEC 60601-1, Medical electrical equipment Part 1: . General requirements for safety (IEC 60601-1:1988/A1:91/A2:95)
- IEC 60601-2-10, Medical electrical equipment Part 2-10: Particular . requirements for the safety of nerve and muscle stimulators
- IEC 60601-1-2, Medical electrical equipment Part 1: General . requirements for safety - Collateral standard: Electromagnetic compatibility -Requirements and tests

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Image /page/2/Picture/1 description: The image shows the seal of the Department of Health & Human Services USA. The seal features a stylized eagle with three tail feathers, representing the department's commitment to health, services, and human well-being. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" are arranged in a circular pattern around the eagle.

Food and Drug Administration 10903 New Hampshire Avenue Document Contro} Room -WO66-G609 Silver Spring, MD 20993-0002

Won Industrial Co. % PATS Corporation Mr. Brandon Choi 205 S. Broadway, Suite 718 Los Angeles, CA 90012

JAN 2 8 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 - 2 -

Re: K102319

Trade/Device Name: Compressible Limb Therapy System WIC-2008 Regulation Number: 21 CFR 890.5650 Regulation Name: Powered inflatable tube massager Regulatory Class: Class II Product Code: IRP Dated: January 20, 2011 Received: January 25, 2011

Dear Mr. Choi:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act (Act do not require approval of a provisions of the Pederal Food, Drug,
You may, therefore, market the desires and in a premarket approval application ( You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misling and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you; however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations of class III (PMA)
found in the Code of Foderal Parchives Titler Titler affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act

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or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm fou the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (2) CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

Sincerely yours.

A. B. R.
for.

Mark N. Melkerson Director Division of Surgical, Orthopedic and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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# Indications for Use

<102319 510(k) Number (if known):

Device Name: Compressible limb therapy system WIC-2008

Indications for Use: WIC-2008 is intended for use by medical professionals and patients at home, who are under medical supervision, in treating many conditions, such as : Primary lymphedema, Edema following trauma and sport injuries, Postimmobilization edema, Venous insufficiencies, Lymphedema.

Prescription Use AND/OR Subpart D) (21 CFR 801 Subpart C) Over-The-Counter Use ________ (Part 21 CFR 801

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

(Division Sign-Off)

Division of Surgical, Orthopedic, and Restorative Devices

510(k) Number K102319