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Cision Vision

Cision Vision, Inc. · Model Cision InVision · UDI-DI 00850059951002

IBM
1
510(k) clearances
0
Adverse events
1
Recalls
14
Facilities

Recalls

DateFirmReason
2013-02-22Aperio Technologies IncAperio initiated this recall because the User Guides incorrectly state the devices had been cleared for specific applications. The User Guides should state the devices are for Rese

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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.