FDA Device Intelligence
HomeDevice types › NPF

Monitor, Apnea, Home Use

FDA product code NPF · Class 2 · Anesthesiology

6
Registered devices
54
Adverse events
3
Recalls
2
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2014-04-29Childrens Medical VenturesThe battery pack wire harness is improperly assembled rendering the device inoperable. The wiring issue causes an error code to be displayed and results in the
2007-10-15Respironics, Inc.Foreign material: Glass fragments may present in the plastic bag material used to ship components.
2007-10-15Respironics, Inc.Foreign material: Glass fragments may present in the plastic bag material used to ship components.

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