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Prosomnus IA MicrO2 with Patient Monitoring

PROSOMNUS SLEEP TECHNOLOGIES · Model MicrO2 with Monitoring · UDI-DI 00863039000447

PLC Prescription
10
510(k) clearances
4
Adverse events
0
Recalls
7
Facilities

Description

Obstructive Sleep Apnea Device with twin mated posts and Patient Monitoring

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.