{
  "snapshot_date": "2026-08-21",
  "product_code": "OAP",
  "query_url": "https://api.fda.gov/device/510k.json?search=product_code:OAP&limit=1000",
  "raw_file_sha256": "511718a26c11d06846a10db19847642b1e11a4a9df08b5ec1ad3799013b07d97",
  "total_records": 112,
  "earliest_decision_date": "2007-01-18",
  "latest_decision_date": "2026-07-17",
  "records_since_2021": 43,
  "records_since_2024": 22,
  "by_clearance_type": {
    "Special": 15,
    "Traditional": 97
  },
  "distinct_applicants": 59,
  "method": "Every number above is computed from the frozen snapshot file whose sha256 is recorded here, not from a live API call. 'records_since_YYYY' counts records with decision_date on or after 1 January of that year. A 510(k) record is a clearance decision, not a product, and not a statement about efficacy."
}
