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Airgle Corporation · Model AF900T · UDI-DI 00860013509934

FRA
10
510(k) clearances
12
Adverse events
0
Recalls
15
Facilities

Description

This Titanium Pro UV module is a replacement accessory for AG900, covered under AG900’s 510(k) K232645. It does not have a separate 510(k).

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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.