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FDA 510(k)

EVERCROSS 0.035 OTW PTA DILATATION CATHETER

K-Number: K110319 · 2011-04-14

ApplicantEv3, Inc.
Decision Date2011-04-14
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EVERCROSS 0.035 OTW PTA DILATATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Ev3, Inc.. It received FDA 510(k) clearance on 2011-04-14 under 510(k) number K110319. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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