{"id":"b0a70caf-648f-49e4-9bfb-057bd32e4a04","slug":"butterfly-iq-plus-fda-510k-k232808","filingNumber":"K232808","filingType":"fda_510k","jurisdiction":"us_fda","applicantCompanyId":"10c41dfa-9a1d-4e6a-a63a-901375715bd7","filingDate":"2023-01-01T00:00:00.000Z","decisionDate":"2023-01-01T00:00:00.000Z","status":"cleared","clearanceScope":"FDA 510(k) K232808 for Butterfly iQ3 Ultrasound System (also covers iQ/iQ+). Portable handheld POCUS. Original iQ cleared 2018.","sources":[{"url":"https://www.accessdata.fda.gov/cdrh_docs/pdf23/K232808.pdf","title":"K232808 510(k)","sourceName":"FDA"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":null,"reviewStatus":"unreviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-07-15T02:42:57.503Z","updatedAt":"2026-07-15T02:42:57.503Z","applicantCompany":{"id":"10c41dfa-9a1d-4e6a-a63a-901375715bd7","slug":"butterfly-network","name":"Butterfly Network"},"modelLinks":[{"id":"06b84f05-26fe-486f-93b6-8d6b379c9225","modelId":"aed64d0b-bb26-4f48-8a32-1a6a7187fdbd","regulatoryFilingId":"b0a70caf-648f-49e4-9bfb-057bd32e4a04","createdAt":"2026-07-15T02:42:58.383Z","model":{"slug":"butterfly-iq-plus","modelName":"Butterfly iQ+"}}]}