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Ir Laser Illuminator Only/Night Vision System

FDA product code REX · Class N · Unknown

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Registered devices
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Adverse events
1
Recalls
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510(k) clearances

Recent recalls

DateFirmReason
2010-01-21Lockheed Martin Gyrocam Systems, Inc.These camera systems were manufactured by LMGS and found to fail to comply with the FDA laser performance standard during an FDA inspection. These camera syst

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