{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
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      "summary_malfunction_reporting": "Eligible",
      "product_code": "MUU",
      "openfda": {
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        "registration_number": [
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      "review_panel": "SU",
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      "device_name": "System, Suction, Lipoplasty",
      "review_code": "",
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      "medical_specialty_description": "General, Plastic Surgery",
      "device_class": "2",
      "definition": "See Federal Register Notice at 86 FR 50887 “Consolidation of Devices That Process Autologous Human Cells, Tissues, and Cellular and Tissue-Based Products at the Point of Care to Produce a Therapeutic Article” (FRN) (FDA-2021-N-0881).",
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