Nxstage Medical, Inc. is one of 5511 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
51
Total
51
Cleared
0
Denied
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.
FDA 510(k) Regulatory Record - Nxstage Medical, Inc.
51 devices
Cleared
Mar 14, 2024
NxStage System One with Cartridge Express (CAR-170-E and CAR-172-E)
Gastroenterology & Urology
184d
Cleared
Jan 18, 2024
NxStage PureFlow Solution
Gastroenterology & Urology
112d
Cleared
Aug 11, 2023
VersiHD with GuideMe software
Gastroenterology & Urology
157d
Cleared
Aug 09, 2019
NxStage Cartridge Express with Speedswap
Gastroenterology & Urology
267d
Cleared
Sep 26, 2018
NxStage Connected Health System
Gastroenterology & Urology
62d
Cleared
Aug 24, 2017
NxStage System One
Gastroenterology & Urology
108d
Cleared
May 09, 2017
NxStage System One Plus
Gastroenterology & Urology
82d
Cleared
Jun 04, 2015
NxStage System One
Gastroenterology & Urology
101d
Cleared
Mar 20, 2015
NxStage Therapeutic Plasma Exchange (TPE) Cartridge
Gastroenterology & Urology
121d
Cleared
Dec 19, 2014
NXSTAGE SYSTEM ONE
Gastroenterology & Urology
172d
Cleared
Sep 11, 2014
MEDISYSTEMS ONESITE DUAL LUMEN NEEDLE WITH MASTERGUARD ANTI-STICK NEEDLE...
Gastroenterology & Urology
255d
Cleared
Jun 16, 2014
NXSTAGE EXPRESS FLUID WARMER
Gastroenterology & Urology
97d
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