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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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4 records meeting your search criteria returned- Product Code: FQO Product Problem: Therapeutic or Diagnostic Output Failure Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
STERIS CORPORATION STERIS 04/22/2021
STERIS CORPORATION - MONTGOMERY 4085 SURGICAL TABLE 01/13/2021
GCX CORPORATION SKYTRON 01/11/2021
STERIS CORPORATION - MONTGOMERY 3085 SP SURGICAL TABLE 05/22/2019
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