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Argus ll Touch Screen Monitor

Second Sight Medical Products, Inc. · Model 014932-001 · UDI-DI 00856264005462

NBF
0
510(k) clearances
93
Adverse events
0
Recalls
1
Facilities

Description

Used during the camera alignment procedure or other tests to record the patient’s responses.

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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.