VASCULAIRE COMPRESSION SYSTEM
K-Number: K103113 · 2011-02-02
Advertisement
Device Summary
Frequently Asked Questions
What is the VASCULAIRE COMPRESSION SYSTEM?
VASCULAIRE COMPRESSION SYSTEM is a medical device that received FDA 510(k) clearance on 2011-02-02. The listed applicant is Venous Health Systems, Inc.. The 510(k) number is K103113.
When did VASCULAIRE COMPRESSION SYSTEM receive FDA 510(k) clearance?
VASCULAIRE COMPRESSION SYSTEM received FDA 510(k) clearance on 2011-02-02, under 510(k) number K103113.
Who is the listed applicant for VASCULAIRE COMPRESSION SYSTEM?
The FDA 510(k) record lists Venous Health Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VASCULAIRE COMPRESSION SYSTEM?
The FDA product code for VASCULAIRE COMPRESSION SYSTEM is JOW.
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 Venous Health Systems, 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: JOW)
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.
Advertisement