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)

VESOFLOW

K-Number: K110977 · 2011-08-25

Decision Date2011-08-25
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VESOFLOW is the device name listed in this FDA 510(k) record. The listed applicant is Caremed Supply, Inc.. It received FDA 510(k) clearance on 2011-08-25 under 510(k) number K110977. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VESOFLOW?

VESOFLOW is a medical device that received FDA 510(k) clearance on 2011-08-25. The listed applicant is Caremed Supply, Inc.. The 510(k) number is K110977.

When did VESOFLOW receive FDA 510(k) clearance?

VESOFLOW received FDA 510(k) clearance on 2011-08-25, under 510(k) number K110977.

Who is the listed applicant for VESOFLOW?

The FDA 510(k) record lists Caremed Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VESOFLOW?

The FDA product code for VESOFLOW 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 Caremed Supply, 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.

↑