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FDA 510(k)

TOP VENULA I.V. CATHETER SET

K-Number: K832624 · 1983-11-21

ApplicantTop Surgical Manufacturers Co.
Decision Date1983-11-21
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TOP VENULA I.V. CATHETER SET is the device name listed in this FDA 510(k) record. The listed applicant is Top Surgical Manufacturers Co.. It received FDA 510(k) clearance on 1983-11-21 under 510(k) number K832624. 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 TOP VENULA I.V. CATHETER SET?

TOP VENULA I.V. CATHETER SET is a medical device that received FDA 510(k) clearance on 1983-11-21. The listed applicant is Top Surgical Manufacturers Co.. The 510(k) number is K832624.

When did TOP VENULA I.V. CATHETER SET receive FDA 510(k) clearance?

TOP VENULA I.V. CATHETER SET received FDA 510(k) clearance on 1983-11-21, under 510(k) number K832624.

Who is the listed applicant for TOP VENULA I.V. CATHETER SET?

The FDA 510(k) record lists Top Surgical Manufacturers Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOP VENULA I.V. CATHETER SET?

The FDA product code for TOP VENULA I.V. CATHETER SET 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 Top Surgical Manufacturers Co. 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.

K844343TOP SINGLE USE U.T.W. A-V FISTULA NEEDLE Y TYPEK843415TOP HYPODERMIC SYRINGE LUER LOCKK843313TOP DISPOSABLE SPINAL NEEDLEK843414TOP HYPODERMIC SYRINGE PISTONK841119TOPS DISPOS. INFUSION SET/HEMODIALYSISK841025TOP DISPOSABLE INFUSION SET

View all 12 devices →

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

View on FDA Database →

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

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