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HEPA Filter

WESTMED, INC. · Model 6234 · UDI-DI 00709078001567

MOD Prescription
1
510(k) clearances
19
Adverse events (1 deaths)
1
Recalls
8
Facilities

Description

w/o CO2 Port

Recalls

DateFirmReason
2005-06-08Medical Device Group Inc.Device separation presenting a choking hazard.

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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.