FDA Device Intelligence
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Computer, Blood-Pressure

FDA product code DSK · Class 2 · Cardiovascular

477
Registered devices
546
Adverse events
1
Recalls
77
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2012-05-04Argon Medical Devices, IncSome of the kits may exhibit a potential defect with the pouch seal. The pouch issue may compromise the sterile barrier.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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