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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

    K043092

    Cited as predicate by: K111330, K120318, K141293

    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
    2024-03-14NAINo action indicatedMidmark Corporation0
    2018-04-02VAIVoluntary action indicatedMidmark Corporation1
    2018-04-02VAIVoluntary action indicatedMidmark Corporation1
    2017-08-22NAINo action indicatedMidmark Corporation0
    2016-12-09NAINo action indicatedMidmark Corporation0
    2016-12-09NAINo action indicatedMidmark Corporation0
    2014-06-09VAIVoluntary action indicatedMidmark Corporation8
    2014-06-09VAIVoluntary action indicatedMidmark Corporation8
    2012-06-28VAIVoluntary action indicatedMidmark Corporation4
    2012-06-28VAIVoluntary action indicatedMidmark Corporation4
    2012-03-13VAIVoluntary action indicatedMidmark Corporation2
    2011-12-28WLWarning LetterMidmark Corporation—
    2011-12-28WLWarning LetterMidmark Corporation—
    2011-09-12OAIOfficial action indicatedMidmark Corporation8
    2011-09-12OAIOfficial action indicatedMidmark Corporation8
    2010-02-24VAIVoluntary action indicatedMidmark Corporation2
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