MEDIVALVE ACWIRE
K-Number: K132545 · 2013-11-08
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Device Summary
Frequently Asked Questions
What is the MEDIVALVE ACWIRE?
MEDIVALVE ACWIRE is a medical device that received FDA 510(k) clearance on 2013-11-08. The listed applicant is Medivalve , Ltd.. The 510(k) number is K132545.
When did MEDIVALVE ACWIRE receive FDA 510(k) clearance?
MEDIVALVE ACWIRE received FDA 510(k) clearance on 2013-11-08, under 510(k) number K132545.
Who is the listed applicant for MEDIVALVE ACWIRE?
The FDA 510(k) record lists Medivalve , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDIVALVE ACWIRE?
The FDA product code for MEDIVALVE ACWIRE is DQX.
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.
Related Devices (Code: DQX)
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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