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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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2 records meeting your search criteria returned- Product Code: KQS Report Date From: 1/1/2020 Report Date To: 12/31/2020
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ManufacturerBrand NameDate Report Received
DORNIER MEDTECH SYSTEMS GMBH DORNIER MEDTECH OPUS II 11/06/2020
DORNIER GENESIS / DORNIER MEDTECH SYSTEM DMT CYSTO TABLE 07/24/2020
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