{
  "format": "devicerts.device.v1",
  "cite_as": "Wizair Compression System, Medical Compression Systems (Dbn), Ltd. deviCERTS medical device catalogue. https://devicerts.com/devices/wizair-compression-system-jow (data as of 2026-11-15).",
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    "json_url": "https://devicerts.com/devices/wizair-compression-system-jow.json",
    "markdown_url": "https://devicerts.com/devices/wizair-compression-system-jow.md",
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    "data_sources": [
      {
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    "status_as_of": "2026-11-15",
    "license": "CC BY 4.0",
    "license_url": "https://creativecommons.org/licenses/by/4.0/",
    "license_scope": "The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.",
    "attribution": "DevicErts, https://devicerts.com/devices/wizair-compression-system-jow",
    "disclaimer": "Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails."
  },
  "device": {
    "name": "Wizair Compression System",
    "registry_name": "WIZAIR COMPRESSION SYSTEM",
    "url": "https://devicerts.com/devices/wizair-compression-system-jow",
    "manufacturer": {
      "name": "Medical Compression Systems (Dbn), Ltd.",
      "url": "https://devicerts.com/manufacturers/medical-compression-systems-dbn-ltd",
      "country": "Israel",
      "country_basis": "FDA 510(k) applicant",
      "fda_registration_country": null
    },
    "status": {
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      "label": "Active",
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        "system": "US FDA"
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          {
            "value": "K023573",
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        ]
      }
    ],
    "product_codes": [
      "JOW"
    ],
    "emdn": [],
    "gmdn": [],
    "description": {
      "text": "The WIZAIR COMPRESSION SYSTEM is a groundbreaking cardiovascular compression device that has been substantially equivalent to the ISO 11613-1 standard for over two decades. Our device has undergone rigorous testing and has been certified by regulatory authorities around the world, ensuring its safety and efficacy. With its advanced technology and user-friendly design, this device is an ideal solution for medical professionals looking to provide high-quality compression therapy.",
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      "note": null
    },
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  },
  "authorizations": [
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      "region": "United States",
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      "number": "K023573",
      "number_label": null,
      "device_udi_di": null,
      "date": "2002-11-21",
      "date_kind": "decision",
      "decision_code": "SESE",
      "expires": null,
      "withdrawn": null,
      "status": "Active",
      "status_note": null,
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    }
  ],
  "no_longer_listed_by": [],
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  "recalls": [
    {
      "number": "Z-0387-2012",
      "classification": "",
      "status": "terminated",
      "initiated": "2011-08-28",
      "reason": "This voluntary field action is being undertaken because MCS has received a limited number of reports involving the use of a non-MCS AC/DC adaptor with the ActiveCare DVT and ActiveCare+S.F.T. devices. The firm found that an ActiveCare DVT device may work improperly if connected to a non-MCS AC/DC adaptor with a higher nominal voltage.  As specified in each product's User Manual, the ActiveCare DVT",
      "applies": "this device",
      "via": "K023573"
    }
  ],
  "eu_market_availability": null,
  "properties": [
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}