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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

No adverse-event reports are linked to this device.

Recall history

No recalls linked.

Regulatory clearances

    Predicate lineage

    K071073

    Cited as predicate by: K143676, K190008, K200494

    Lineage each submission cites, walked transitively (indented = the cited device's own predicates). Extracted from public 510(k) summary text — heuristic, and includes reference devices mentioned alongside true predicates.

    Manufacturer compliance record
    DateTypeOutcomeFacilityCitations
    2018-07-19VAIVoluntary action indicatedGE Medical Systems Information Technologies, Inc.5
    2016-04-28NAINo action indicatedGE Medical Systems Information Technologies0
    2013-09-25VAIVoluntary action indicatedGE Medical Systems Information Technologies, Inc.5
    2013-05-14VAIVoluntary action indicatedGE Medical Systems Information Technologies0
    2012-10-09VAIVoluntary action indicatedGE Medical Systems Information Technologies, Inc.6
    2010-08-20NAINo action indicatedGE Medical Systems Information Technologies, Inc.0
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