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Polysmith Version 12.0
Neurotronics, LLC · Model 12.0 · UDI-DI 00817111021172
10
510(k) clearances
10
Adverse events
0
Recalls
24
Facilities
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Get your free API keyRead the docsData 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.
