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Gases Used Within Eye To Place Pressure On Detached Retina

FDA product code LPO · Class 3 · Ophthalmic

28
Registered devices
504
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2003-11-18Alcon Laboratories, IncThe firm initiated the recall on 11/18/2003 via letters to all consignees. The letter advises physicians to stop using any patient bracelets (blue color) that

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.