← Product Code [JOW](/submissions/CV/subpart-f%E2%80%94cardiovascular-therapeutic-devices/JOW) · K120972 # FLEXITOUCH SYSTEM (K120972) _Tactile Systems Technology, Inc. · JOW · Apr 13, 2012 · Cardiovascular · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/CV/subpart-f%E2%80%94cardiovascular-therapeutic-devices/JOW/K120972 ## Device Facts - **Applicant:** Tactile Systems Technology, Inc. - **Product Code:** [JOW](/submissions/CV/subpart-f%E2%80%94cardiovascular-therapeutic-devices/JOW.md) - **Decision Date:** Apr 13, 2012 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 870.5800 - **Device Class:** Class 2 - **Review Panel:** Cardiovascular - **Attributes:** Therapeutic, 3rd-Party Reviewed ## Indications for Use The Flexitouch® system is intended for use by medical professionals and patients who are under medical supervision, in treating many conditions such as: - Primary lymphedema . - Post mastectomy edema . - Edema following trauma and sports injuries - Post immobilization edema ● - . Venous insufficiencies - Lymphedema. . - Reducing wound healing time . - Treatment and assistance in healing: stasis dermatitis; venous stasis ulcers; arterial and diabetic leg ulcers ## Device Story Flexitouch® system is a prescription pneumatic compression device; consists of garment set and pneumatic sequential controller. Garments wrap around affected body regions; multiple chambers fill with air to provide low-level compression. Used in clinical or home settings by medical professionals or patients under medical supervision. Device applies sequential pneumatic pressure to treat edema and assist in wound healing. Healthcare providers use output to manage lymphedema and venous conditions; patient benefits include reduced edema and improved wound healing outcomes. ## Clinical Evidence Bench testing only. Evidence includes software validation, device performance testing, and device hazard analysis (risk assessment and FMEA). Product shipping tests conducted per ASTM D4169. ## Technological Characteristics Pneumatic compression system; consists of garment set and pneumatic sequential controller. Multi-chambered garments provide low-level air-filled compression. Compliant with IEC 60601-1 (safety) and EN 60601-1-2 (EMC). Quality management per ISO 13485. Shipping tested per ASTM D4169. ## Regulatory Identification A compressible limb sleeve is a device that is used to prevent pooling of blood in a limb by inflating periodically a sleeve around the limb. ## Predicate Devices - Flexitouch® system Model PD32-120 ([K013061](/device/K013061.md)) - Flexitouch® system ([K062818](/device/K062818.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ APR 1 3 2012 K120972 pg 1 of 2 ## Section 5 - 510(k) Summary | Submission Date: | 15 February 2012 | |-------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Submitter: | Phillip R. Rose
Director of Quality Systems and Regulatory Affairs
Tactile Systems Technology, Inc.
1331 Tyler Street NE, Suite 200
Minneapolis, MN 55413
Phone: (612) 355-5100 | | Contact person: | Phillip R. Rose | | Name of Device: | Flexitouch® system | | Classification: | Compressible Limb Sleeve (21 CFR 870.5800) | | Predicate Device: | Tactile Systems Technology, Inc. Flexitouch® system Model
PD32-120 (K013061) and subsequent 510(k) (K062818) for
additional indication for use. | #### Description of Device: The Flexitouch® system is a prescription pneumatic compression system consisting of a garment set and a pneumatic sequential controller. The garments are wrapped around the affected body regions so that the garment fits snugly. The garments have multiple chambers that are filled with air to provide for low-level compression in the treated areas. #### Intended Use: The Flexitouch® system is intended for use by medical professionals and patients at home who are under medical supervision in treating many conditions such as: - Primary lymphedema . - Post mastectomy edema . - Edema following trauma and sports issues . - Post immobilization edema . - Venous insufficiencies . - Lymphedema . - . Reducing wound healing time - Treatment and assistance in healing: stasis dermatitis; venous stasis ulcers; . arterial and diabetic leg ulcers {1}------------------------------------------------ #### Comparison of Technological Characteristics: The Flexitouch® system has the same technological characteristics to the predicate device with respect to: - intended use . - . performance - . design - materials used . - construction . - energy source . - sterility . - labeling . and raises no new safety and/or effectiveness concerns. #### Summary of Testing to Internationally Recognized Standards: The Flexitouch® system has been tested and certified compliant to the following standards: - IEC 60601-1: Medical Electrical Equipment General Requirements for Safety . - EN 60601-1-2:Medical Electrical Equipment General Requirements for Safety . Electromagnetic Compatibility - ISO 13485: Medical Devices Quality Management Systems-● Requirements for Regulatory Purposes - 93/42/EEC: Medical Devices Directive CE Marking . #### Summary of Additional Performance Testing: Comparative performance testing and evaluation was successfully completed to verify the substantial equivalence between the Flexitouch® system, and the predicate device. This includes: - Software validation testing, . - Device performance testing . - Device Hazard Analysis � - o Risk assessment - o Design and process FMEA. - Product shipping tests per ASTM D4169 . ### Substantial Equivalence Conclusion: Device testing and evaluation has demonstrated that the Flexitouch® system raises no new safety and/or effectiveness concerns and is substantially equivalent to the predicate device. {2}------------------------------------------------ ### DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002 APR 1 3 2012 Tactile System Technology, Inc. c/o Mr. Ned Devine Underwriters Laboratories, Inc. 333 Pfingsten Road Northbrook, IL 60062 Re: K120972 Trade/Device Name: Flexitouch® System Regulation Number: 21 CFR 870.5800 Regulation Name: Compressible Limb Sleeves Regulatory Class: Class II Product Code: JOW Dated: March 29, 2012 Received: April 2. 2012 Dear Mr. Devine: 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) that do not require approval of a premarket approval application (PMA). 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 misbranding 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 affecting your device can be {3}------------------------------------------------ #### Page 2 - Mr. Ned Devine 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 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 11 70 http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for 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" (21CFR 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/ReportalProblem/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 I va may overs International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Sincerely vours. M. A. Wilhelm - Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ ## Section 4 - Indications for Use Statement # Indications for Use K 120972 510(k) Number (if known): Device Name: Flexitouch® system Indications For Use: The Flexitouch® system is intended for use by medical professionals and patients who are under medical supervision, in treating many conditions such as: - Primary lymphedema ● - Post mastectomy edema . - Edema following trauma and sports injuries - Post immobilization edema ● - . Venous insufficiencies - Lymphedema. . - Reducing wound healing time . - Treatment and assistance in healing: stasis dermatitis; venous stasis ulcers; arterial and diabetic leg ulcers Prescription Use X (Part 21 CFR 801 Subpart D) OR Over the Counter Use (21 CFR 801 Subpart C) ### (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) M & - William ---------------------------------------------------------------------------------------------------------------------------------------------- | (Division Sign-Off) | |------------------------------------| | Division of Cardiovascular Devices | K120972 Page 7 of 120 510(k) Number --- **Source:** [https://fda.innolitics.com/submissions/CV/subpart-f%E2%80%94cardiovascular-therapeutic-devices/JOW/K120972](https://fda.innolitics.com/submissions/CV/subpart-f%E2%80%94cardiovascular-therapeutic-devices/JOW/K120972) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com