HydroMID 4F Single Lumen Midline Catheter
K-Number: K220772 · 2022-12-07
Device Summary
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. The listed applicant is Access Vascular, Inc.. The 510(k) number is K220772.
When did HydroMID 4F Single Lumen Midline Catheter receive FDA 510(k) clearance?
HydroMID 4F Single Lumen Midline Catheter received FDA 510(k) clearance on 2022-12-07, under 510(k) number K220772.
Who is the listed applicant for HydroMID 4F Single Lumen Midline Catheter?
The FDA 510(k) record lists Access Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
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
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.
Other records listing Access Vascular, 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.
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.
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.