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ULTRA FLOW

Alcon Laboratories, Inc. · Model 00380658172015 · UDI-DI 00380658172015

NKK Prescription
0
510(k) clearances
7
Adverse events (1 deaths)
0
Recalls
0
Facilities

Description

ULTRAFLOW S/P 45 BENT TIP, .3MM

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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.