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E-Sphyg™ II

AMERICAN DIAGNOSTIC CORP · Model 9002-3-UK · UDI-DI 00634782083366

HLJ
1
510(k) clearances
5
Adverse events
0
Recalls
64
Facilities

Description

AC Adapter-9002,United Kingdom

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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.