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Alice 6

Respironics, Inc. · Model Alice 6 Upgrade, LDx, US · UDI-DI 00606959006089

OLV Prescription
10
510(k) clearances
21
Adverse events
1
Recalls
48
Facilities

Description

Alice 6 LDx polysomnography system, (Alice 5 to 6 conversion/changeover kit), U.S./North America

Recalls

DateFirmReason
2018-02-01Natus Neurology IncPotential to be able to import an ambulatory exam for a patient for which the exam was not started.

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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.