EVERCROSS 0.035 OTW PTA DILATATION CATHETER
K-Number: K110319 · 2011-04-14
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Device Summary
Frequently Asked Questions
What is the EVERCROSS 0.035 OTW PTA DILATATION CATHETER?
EVERCROSS 0.035 OTW PTA DILATATION CATHETER is a medical device that received FDA 510(k) clearance on 2011-04-14. The listed applicant is Ev3, Inc.. The 510(k) number is K110319.
When did EVERCROSS 0.035 OTW PTA DILATATION CATHETER receive FDA 510(k) clearance?
EVERCROSS 0.035 OTW PTA DILATATION CATHETER received FDA 510(k) clearance on 2011-04-14, under 510(k) number K110319.
Who is the listed applicant for EVERCROSS 0.035 OTW PTA DILATATION CATHETER?
The FDA 510(k) record lists Ev3, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EVERCROSS 0.035 OTW PTA DILATATION CATHETER?
The FDA product code for EVERCROSS 0.035 OTW PTA DILATATION CATHETER is LIT.
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 Ev3, 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: LIT)
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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