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Manometer, Blood-Pressure, Venous

FDA product code KRK · Class 2 · Cardiovascular

3
Registered devices
15
Adverse events
2
Recalls
9
510(k) clearances

Devices with this code

Medex — ICU MEDICAL, INC.N/A — CAREFUSION 2200, INCMedex — ICU MEDICAL, INC.

Recent recalls

DateFirmReason
2017-02-23Carefusion 2200 IncThe integrity of the sterile packaging is potentially compromised.
2005-11-18Medex IncThe product is labeled as 'Latex Free' , however,one of the components of the finished product may contain latex.

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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.