Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VARICATH PERIPHERAL INFUSION CATHETER

K-Number: K073400 · 2007-12-20

ApplicantVeinrx, Inc.
Decision Date2007-12-20
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VARICATH PERIPHERAL INFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Veinrx, Inc.. It received FDA 510(k) clearance on 2007-12-20 under 510(k) number K073400. 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 VARICATH PERIPHERAL INFUSION CATHETER?

VARICATH PERIPHERAL INFUSION CATHETER is a medical device that received FDA 510(k) clearance on 2007-12-20. The listed applicant is Veinrx, Inc.. The 510(k) number is K073400.

When did VARICATH PERIPHERAL INFUSION CATHETER receive FDA 510(k) clearance?

VARICATH PERIPHERAL INFUSION CATHETER received FDA 510(k) clearance on 2007-12-20, under 510(k) number K073400.

Who is the listed applicant for VARICATH PERIPHERAL INFUSION CATHETER?

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

What is the FDA product code for VARICATH PERIPHERAL INFUSION CATHETER?

The FDA product code for VARICATH PERIPHERAL INFUSION CATHETER 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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Veinrx, Inc. as applicant

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.

K052738INFUSIONCATH PERIPHERAL INFUSION CATHETER, MODELS VF0012, VF0016, VF0024, VF0028, VF0032, VF0036, VF0040, VF0044

Related Devices (Code: KRA)

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.

K253509TriSalus TriNav Advance Infusion SystemTrisalus Life SciencesK254051Extroducer Infusion Catheter SystemSmartWise Sweden ABK261610Verge™ MicrocatheterInstylla, Inc.K260771TruSelect™ 2.6 MicrocatheterBoston Scientific CorporationK250794InVera Infusion DeviceInvera MedicalK243534Micro 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.

↑