High Pressure Tubing
K-Number: K232388 · 2023-11-21
Decision Date2023-11-21
Product CodeDXT
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
High Pressure Tubing is a medical device manufactured by Ningbo Dizegens Medical Science Co.,Ltd. It received FDA 510(k) clearance on 2023-11-21 under approval number K232388. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the High Pressure Tubing?
High Pressure Tubing is a medical device that received FDA 510(k) clearance on 2023-11-21. It is manufactured by Ningbo Dizegens Medical Science Co.,Ltd. The 510(k) number is K232388.
When was High Pressure Tubing approved by the FDA?
High Pressure Tubing received FDA 510(k) clearance on 2023-11-21, under approval number K232388.
What company makes High Pressure Tubing?
High Pressure Tubing is manufactured by Ningbo Dizegens Medical Science Co.,Ltd.
What is the FDA product code for High Pressure Tubing?
The FDA product code for High Pressure Tubing is DXT.
Related Clinical Trials
Other Devices by Ningbo Dizegens Medical Science Co.,Ltd
Related Devices (Code: DXT)
K152906Disposable High Pressure Injector SyringeWuxi Yushou Medical Appliances Co., Ltd.
K160190Sunmed Control SyringesSunny Medical Device (Shenzhen) Co., Ltd.
K161471MR Syringe Dual Pack for Solaris InjectorsCoeur, Inc.
K161505DyeVert NG Contrast Modulation SystemOsprey Medical, Inc.
K160107DiamondTOUCH Inflation Device and Fluid Dispensing SyringeMerit Medical Systems, Inc.
K152978DeRoyal Angiography KitsDeroyal Industries, Inc.
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.