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Optitrol HEPR-2

Lgc Clinical Diagnostics, Inc. · Model SR12057 · UDI-DI 00850075957002

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510(k) clearances
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Adverse events
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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.