TRAXCESS 0.014 HYDROPHILIC GUIDEWIRE
K-Number: K080863 · 2008-04-17
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Device Summary
Frequently Asked Questions
What is the TRAXCESS 0.014 HYDROPHILIC GUIDEWIRE?
TRAXCESS 0.014 HYDROPHILIC GUIDEWIRE is a medical device that received FDA 510(k) clearance on 2008-04-17. The listed applicant is MicroVention, Inc.. The 510(k) number is K080863.
When did TRAXCESS 0.014 HYDROPHILIC GUIDEWIRE receive FDA 510(k) clearance?
TRAXCESS 0.014 HYDROPHILIC GUIDEWIRE received FDA 510(k) clearance on 2008-04-17, under 510(k) number K080863.
Who is the listed applicant for TRAXCESS 0.014 HYDROPHILIC GUIDEWIRE?
The FDA 510(k) record lists MicroVention, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRAXCESS 0.014 HYDROPHILIC GUIDEWIRE?
The FDA product code for TRAXCESS 0.014 HYDROPHILIC GUIDEWIRE 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.
Other records listing MicroVention, 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: 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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