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KOVA

KOVA INTERNATIONAL, INC. · Model 87146 · UDI-DI 00855617006149

KEW
8
510(k) clearances
44
Adverse events
1
Recalls
104
Facilities

Description

Glasstic Slide 10, 1000 Determinations

Recalls

DateFirmReason
2003-01-29Cytyc CorporationMicroscope Slides contaminated with fungal material

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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.