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KENOREX

KENTRON HEALTHCARE, INC. · Model 779504 · UDI-DI 10852244007362

CAP
1
510(k) clearances
74
Adverse events (10 deaths)
0
Recalls
54
Facilities

Description

RESUSCITATOR MANOMETER 0-60 CMS WATER 30 MM ID

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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.