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FDA 510(k)

HydroMID 4F Single Lumen Midline Catheter

K-Number: K220772 · 2022-12-07

ApplicantAccess Vascular, Inc.
Decision Date2022-12-07
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HydroMID 4F Single Lumen Midline Catheter is a medical device manufactured by Access Vascular, Inc.. It received FDA 510(k) clearance on 2022-12-07 under approval number K220772. 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 HydroMID 4F Single Lumen Midline Catheter?

HydroMID 4F Single Lumen Midline Catheter is a medical device that received FDA 510(k) clearance on 2022-12-07. It is manufactured by Access Vascular, Inc.. The 510(k) number is K220772.

When was HydroMID 4F Single Lumen Midline Catheter approved by the FDA?

HydroMID 4F Single Lumen Midline Catheter received FDA 510(k) clearance on 2022-12-07, under approval number K220772.

What company makes HydroMID 4F Single Lumen Midline Catheter?

HydroMID 4F Single Lumen Midline Catheter is manufactured by Access Vascular, Inc..

What is the FDA product code for HydroMID 4F Single Lumen Midline Catheter?

The FDA product code for HydroMID 4F Single Lumen Midline Catheter is FOZ.

Related Clinical Trials

NCT07475091 Standardizing Swallow Pressure Measurements NOT_YET_RECRUITING NCT07614529 Hyperangulated vs Standard Videolaryngoscopy vs Direct Laryngoscopy for Double-Lumen Endobronchial Tube Intubation NOT_YET_RECRUITING NCT07610681 Midline Catheter Study ACTIVE_NOT_RECRUITING NCT06958731 In-plane Versus Real Time Bi-plane Single-operator Laser-assisted With a Innovative T-shaped Probe for Ultrasound-guided Internal Jugular Vein Catheterization:A Randomized Controlled Trial ENROLLING_BY_INVITATION NCT06735534 Repeat Ablation of Persistent Atrial Fibrillation, Including Mitral Isthmus Catheter Ablation, With the FARAPULSE Pulsed Field Ablation System RECRUITING NCT07095660 RECANA OUS - Recana Thrombectomy Catheter System for Venous Obstruction and Occlusion Study (RECANA-OUS-IRL) RECRUITING

Other Devices by Access Vascular, Inc.

K172885HydroPICC K193015HydroPICC (PICC-142) K203069HydroMID K213550HydroPICC 5F Dual Lumen Catheter K243458HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001302); HydroPICC 4Fr Single Lumen Marked catheter - Maximal Barrier kit (70001304); HydroPICC 5Fr Dual Lumen Marked catheter, 130 cm guidewire - Basic Kit (70002301); HydroPICC 5Fr Dual Lumen Marked catheter, 70 cm guidewire - Basic Kit (70002302); HydroPICC 5Fr Dual Lumen Marked catheter - Maximal Barrier kit (70002304); Hydr K251212Dual Lumen 5Fr HydroPICC Catheter (PICC-251CM) (PICC-251CM); Dual Lumen 5Fr HydroPICC Catheter (PICC-252CM) (PICC-252CM)

View all 9 devices →

Related Devices (Code: FOZ)

K162894AccuCath Intravascular CatheterC.R. Bard, Inc. K161779MedSource TrueSafe Safety IV Catheter, MedSource TrueSafe Comfort Safety IV CatheterMedsource International, LLC K162377PowerGlide Pro Midline CatheterC.R. Bard, Inc. K161866BioFlo Midline CatheterNavilyst Medical, Inc. K161777BD Nexiva and BD Nexiva Diffusics Closed IV Catheter SystemsBecton Dickinson Infusion Therapy Systems, Inc. K160592SUPERCATH 6Togo Medikit Co., Ltd.

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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