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Tissue-Tek® Quick-Ray™

SAKURA FINETEK U.S.A., INC. · Model 8019 · UDI-DI 00615233081827

KER
5
510(k) clearances
4
Adverse events
0
Recalls
28
Facilities

Description

Recipient Block, 5 mm

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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.