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LED Daylite REVEAL

Designs For Vision, Inc. · Model 9500-0000-0000 · UDI-DI 00810070572600

QCR Prescription
1
510(k) clearances
0
Adverse events
0
Recalls
2
Facilities

Description

The REVEAL FC is indicated for use as a wound autofluorescence imaging device to view autofluorescence images from skin wounds that are exposed to its excitation light.

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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.