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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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5 records meeting your search criteria returned- Product Code: KDI Patient Problem: Cough Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 12/29/2021
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 11/03/2021
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 09/13/2021
BAXTER HEALTHCARE CORPORATION REVACLEAR 400 07/12/2021
BAXTER HEALTHCARE CORPORATION REVACLEAR 400 07/09/2021
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