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Excyte®

ELITechGroup B.V. · Model Plastic ESR Vacuum Tube · UDI-DI 03661540700668

GHC
1
510(k) clearances
32
Adverse events
1
Recalls
17
Facilities

Recalls

DateFirmReason
2010-04-12Vital Diagnostics, Inc.The tube may fall out or separate from the Slider adapter

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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.