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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
  • 510(k)K103627Substantially equivalent (SESE) · 2011-10-14clearance family

Predicate lineage

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
2024-06-28VAIVoluntary action indicatedAbbott3
2020-01-10NAINo action indicatedAbbott0
2018-06-22NAINo action indicatedAbbott0
2018-02-01NAINo action indicatedAbbott0
2016-09-16NAINo action indicatedAbbott0
2013-06-13NAINo action indicatedAbbott GmbH0
2013-06-11NAINo action indicatedAbbott0
2013-03-08VAIVoluntary action indicatedAbbott0
2012-02-09NAINo action indicatedAbbott GmbH0
2011-10-05NAINo action indicatedAbbott0
2010-09-23VAIVoluntary action indicatedAbbott GmbH0
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