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Onyx HD 500

Micro Therapeutics, Inc. · Model 105-8101-500 · UDI-DI 00836462005129

OBA Prescription
0
510(k) clearances
15
Adverse events (1 deaths)
0
Recalls
2
Facilities

Description

105-8101-500 ONYX HD500 KIT ANEURYS

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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.