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Perimeter, Automatic, Ac-Powered

FDA product code HPT · Class 1 · Ophthalmic

69
Registered devices
3
Adverse events
1
Recalls
41
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2012-08-17Haag-Streit USA IncThe firm recalled the device after learning of a possible deviation in the stimulus luminance of the Perimeter OCTOPUS 101.

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