FDA 510(k)

MX703 AND MX730 CONTINUOUS FLUSH DEVICES

K-Number: K961527 · 1996-06-06

Decision Date1996-06-06

Product CodeKRA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MX703 AND MX730 CONTINUOUS FLUSH DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1996-06-06 under 510(k) number K961527. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MX703 AND MX730 CONTINUOUS FLUSH DEVICES?

MX703 AND MX730 CONTINUOUS FLUSH DEVICES is a medical device that received FDA 510(k) clearance on 1996-06-06. The listed applicant is Medex, Inc.. The 510(k) number is K961527.

When did MX703 AND MX730 CONTINUOUS FLUSH DEVICES receive FDA 510(k) clearance?

MX703 AND MX730 CONTINUOUS FLUSH DEVICES received FDA 510(k) clearance on 1996-06-06, under 510(k) number K961527.

Who is the listed applicant for MX703 AND MX730 CONTINUOUS FLUSH DEVICES?

The FDA 510(k) record lists Medex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MX703 AND MX730 CONTINUOUS FLUSH DEVICES?

The FDA product code for MX703 AND MX730 CONTINUOUS FLUSH DEVICES is KRA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medex, Inc. as applicant

K042432PHARMGUARD TOOLBOX, MODEL G6000782 K040899MEDEX 3000 SERIES MR SYRINGE INFUSION PUMP K020780TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICP K000328MEDEX 3000 SERIES MRI COMPATIBLE SYRINGE INFUSION PUMP K982640MEDEX 3000 SERIES SYRINGE INFUSION PUMP K982123CONTRAST CONTROL DEVICE

View all 48 devices →

Related Devices (Code: KRA)

K253509TriSalus TriNav Advance Infusion SystemTrisalus Life Sciences K254051Extroducer Infusion Catheter SystemSmartWise Sweden AB K261610Verge™ MicrocatheterInstylla, Inc.K260771TruSelect™ 2.6 MicrocatheterBoston Scientific Corporation K250794InVera Infusion DeviceInvera Medical K243534Micro CatheterSuzhou Zenith Vascular SciTech Limited

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.