inforMED
INQClass I

Table, Powered

Physical Medicine · 21 CFR 890.3760

MDR events47All time
Recalls2All time
Registered firms63Currently listed
510(k) clearances102All time

Product problems

Reported product problem codes, most common first

Improper or Incorrect Procedure or Method6
Device Operates Differently Than Expected4
Unintended Movement4
Adverse Event Without Identified Device or Use Problem3
Device Remains Activated3
Entrapment of Device3
Self-Activation or Keying3
Unintended System Motion3

Trend for “Improper or Incorrect Procedure or Method

No history to chart.

Recalls

2 recall events for this product code

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