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)

COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE

K-Number: K072167 · 2007-09-06

Decision Date2007-09-06
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Vascular Dynamics. It received FDA 510(k) clearance on 2007-09-06 under 510(k) number K072167. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE?

COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE is a medical device that received FDA 510(k) clearance on 2007-09-06. The listed applicant is Advanced Vascular Dynamics. The 510(k) number is K072167.

When did COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE receive FDA 510(k) clearance?

COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE received FDA 510(k) clearance on 2007-09-06, under 510(k) number K072167.

Who is the listed applicant for COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE?

The FDA 510(k) record lists Advanced Vascular Dynamics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE?

The FDA product code for COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE is DXC.

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 Advanced Vascular Dynamics 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: DXC)

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.

↑