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Neuronetics

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories2
Latest FDA decision2023-12-13

SEC Filings: 1 filings on record. Latest: 8-K (2026-07-20). View on SEC EDGAR →

TypeNumberDevice NameCodeDateActions
510(k) K233621 NeuroStar Advanced Therapy System (Version 3.8)OBP2023-12-13 View
510(k) K231350 OCD MT Cap (85-00397-000)QCI2023-06-08 View
510(k) K230029 NeuroStar Advanced Therapy System (Version 3.7)OBP2023-04-04 View

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