Home › AMERICAN DIAGNOSTIC CORP › E-Sphyg™ II
E-Sphyg™ II
AMERICAN DIAGNOSTIC CORP · Model 9002-3-UK · UDI-DI 00634782083366
1
510(k) clearances
5
Adverse events
0
Recalls
64
Facilities
Description
AC Adapter-9002,United Kingdom
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
