Nxstage Medical, Inc. is one of 5669 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nxstage Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NxStage System One with Cartridge Express (CAR-170-E and CAR-172-E), NxStage PureFlow Solution, VersiHD with GuideMe software
Nxstage Medical, Inc. has 51 FDA 510(k) cleared gastroenterology & urology devices. Based in Tewksburt, US.
Latest FDA clearance: Mar 2024. Active since 2001.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Nxstage Medical, Inc.
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