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FDA 510(k)

ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY

K-Number: K944660 · 1995-03-13

ApplicantNeostar Medical Technologies, Inc.
Decision Date1995-03-13
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Neostar Medical Technologies, Inc.. It received FDA 510(k) clearance on 1995-03-13 under 510(k) number K944660. 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 ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY?

ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY is a medical device that received FDA 510(k) clearance on 1995-03-13. The listed applicant is Neostar Medical Technologies, Inc.. The 510(k) number is K944660.

When did ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY receive FDA 510(k) clearance?

ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY received FDA 510(k) clearance on 1995-03-13, under 510(k) number K944660.

Who is the listed applicant for ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY?

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

What is the FDA product code for ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY?

The FDA product code for ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY 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 Neostar Medical Technologies, 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.

K960625SPREADABLE SHEATH INTRODUCER SETK944511ACUTE CENTRAL VENOUS ACCESS CATHETER (ACVAC)K941851DUAL LUMEN CATHETER (DLC) TRAY

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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