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LTV

VYAIRE MEDICAL, INC. · Model 466631 · UDI-DI 10190752173545

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

Description

ELECTRODES BLUE SENSOR DISP WET GEL

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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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.