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FDA 510(k)

ABLE CENTRAL VENOUS CATHETER

K-Number: K070451 · 2007-07-31

ApplicantFoshan Nanhai Bai HE Medical Technology Co., Ltd.
Decision Date2007-07-31
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ABLE CENTRAL VENOUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Foshan Nanhai Bai HE Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2007-07-31 under 510(k) number K070451. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABLE CENTRAL VENOUS CATHETER?

ABLE CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 2007-07-31. The listed applicant is Foshan Nanhai Bai HE Medical Technology Co., Ltd.. The 510(k) number is K070451.

When did ABLE CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?

ABLE CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 2007-07-31, under 510(k) number K070451.

Who is the listed applicant for ABLE CENTRAL VENOUS CATHETER?

The FDA 510(k) record lists Foshan Nanhai Bai HE Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ABLE CENTRAL VENOUS CATHETER?

The FDA product code for ABLE CENTRAL VENOUS CATHETER is FOZ.

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 Foshan Nanhai Bai HE Medical Technology Co., Ltd. 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.

K102833DISPOSABLE HEMODIALYSIS ACCESS CATHETER SETS

Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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