VENOTRAIN CURAFLOW
K-Number: K111662 · 2011-10-04
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Device Summary
Frequently Asked Questions
What is the VENOTRAIN CURAFLOW?
VENOTRAIN CURAFLOW is a medical device that received FDA 510(k) clearance on 2011-10-04. The listed applicant is Bauerfeind AG. The 510(k) number is K111662.
When did VENOTRAIN CURAFLOW receive FDA 510(k) clearance?
VENOTRAIN CURAFLOW received FDA 510(k) clearance on 2011-10-04, under 510(k) number K111662.
Who is the listed applicant for VENOTRAIN CURAFLOW?
The FDA 510(k) record lists Bauerfeind AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VENOTRAIN CURAFLOW?
The FDA product code for VENOTRAIN CURAFLOW is DWL.
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 Bauerfeind AG 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: DWL)
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.
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