FDA Device Intelligence
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Manometer, Spinal-Fluid

FDA product code FMJ · Class 2 · General Hospital

44
Registered devices
411
Adverse events
5
Recalls
6
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-02-22Busse Hospital Disposables, Inc.Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a dru
2004-09-09Smiths Medical ASD, Inc.Sterility of the device is compromised due to packaging defects
2004-09-09Smiths Medical ASD, Inc.Sterility of the device is compromised due to packaging defects
2004-09-09Smiths Medical ASD, Inc.Sterility of the device is compromised due to packaging defects
2004-09-09Smiths Medical ASD, Inc.Sterility of the device is compromised due to packaging defects

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