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Alpha-Tec Systems

Alpha-TEC Systems, Inc. · Model 0 · UDI-DI 00816085020105

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

Description

CELL-BOND Slide, 1 Red well, no background

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.