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)

VITAFLON PLUS/VASCULON

K-Number: K941417 · 1994-10-06

ApplicantHogan & Hartson
Decision Date1994-10-06
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAFLON PLUS/VASCULON is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1994-10-06 under 510(k) number K941417. 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 VITAFLON PLUS/VASCULON?

VITAFLON PLUS/VASCULON is a medical device that received FDA 510(k) clearance on 1994-10-06. The listed applicant is Hogan & Hartson. The 510(k) number is K941417.

When did VITAFLON PLUS/VASCULON receive FDA 510(k) clearance?

VITAFLON PLUS/VASCULON received FDA 510(k) clearance on 1994-10-06, under 510(k) number K941417.

Who is the listed applicant for VITAFLON PLUS/VASCULON?

The FDA 510(k) record lists Hogan & Hartson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITAFLON PLUS/VASCULON?

The FDA product code for VITAFLON PLUS/VASCULON 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 Hogan & Hartson 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.

K974168COOPERSURGICAL INFRARED COAGULATORK973849BIOABSORBABLE BANKART TACKK973162DUAL RADIATION TARGETING SYSTEM DRTS DRAPEK950169RIBOSOMAL P EIA TEST SYSTEMK942389TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVESK946217CARDIOLIPIN M EIA TEST SYSTEM

View all 26 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.

↑