Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing
K-Number: K151932 · 2016-03-31
ApplicantStryker Corporation
Decision Date2016-03-31
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing is a medical device manufactured by Stryker Corporation. It received FDA 510(k) clearance on 2016-03-31 under approval number K151932. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing?
Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing is a medical device that received FDA 510(k) clearance on 2016-03-31. It is manufactured by Stryker Corporation. The 510(k) number is K151932.
When was Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing approved by the FDA?
Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing received FDA 510(k) clearance on 2016-03-31, under approval number K151932.
What company makes Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing?
Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing is manufactured by Stryker Corporation.
What is the FDA product code for Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing?
The FDA product code for Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing is HRX.
Related Clinical Trials
NCT02746458
Rehabilitation Enhanced by Partial Arterial Inflow Restrictions
COMPLETED
NCT06941558
The UK ADAPTIS Study
ACTIVE_NOT_RECRUITING
NCT05588011
Influence of Oxygenator Selection on Platelet Function and Rotational Thromboelastometry Following Cardiopulmonary Bypass
COMPLETED
NCT04214535
Anterior Cervical Disectomy And Fusion Using The Tritanium® C Anterior Cervical Cage For One Or Two-Levels
ACTIVE_NOT_RECRUITING
Other Devices by Stryker Corporation
Related Devices (Code: HRX)
K162062AVAmax Vertebral Balloon, AVAflex Vertebral BalloonStryker Corporation
K161878PORTAGE SystemBaylis Medical Company, Inc.
K162475mi-eye 2, mi-eye 2 monitorTrice Medical
K152511Neo - Arthroscope (Rigid) 2.0mm/3.5mm, Outer sheath/ cannula, Outer sheath/ cannula w/ Handle, Trocar for outersheath/ cannulaProsurg, Inc.
K160249ULTRA TelescopesOlympus Winter & Ibe GmbH
K151268SPINAUT-V, SPINAUT-S, SPINAUT-IImedicom Co., Ltd.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.