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Peripheral Electromagnetic Field (Pemf) To Aid Wound Healing

FDA product code MBQ · Class 3 · Unknown

0
Registered devices
2
Adverse events
2
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2017-12-29Toshiba American Medical Systems IncDuring an examination a device error occurred and the ceiling drive operation was disabled. It was found that the fastening bolts of the driving portion of the
2006-09-01AGFA Corp.Users may experience one or more of four (4) problems; 1. Image quality problem with full leg full spine exams. 2. Unable to print 2 or more images on 1 film. 3

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