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FDA 510(k)

VEINNOVATIONS INFILTRATION SYSTEM

K-Number: K050474 · 2005-04-14

ApplicantVeinnovations, LLC
Decision Date2005-04-14
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VEINNOVATIONS INFILTRATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Veinnovations, LLC. It received FDA 510(k) clearance on 2005-04-14 under 510(k) number K050474. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEINNOVATIONS INFILTRATION SYSTEM?

VEINNOVATIONS INFILTRATION SYSTEM is a medical device that received FDA 510(k) clearance on 2005-04-14. The listed applicant is Veinnovations, LLC. The 510(k) number is K050474.

When did VEINNOVATIONS INFILTRATION SYSTEM receive FDA 510(k) clearance?

VEINNOVATIONS INFILTRATION SYSTEM received FDA 510(k) clearance on 2005-04-14, under 510(k) number K050474.

Who is the listed applicant for VEINNOVATIONS INFILTRATION SYSTEM?

The FDA 510(k) record lists Veinnovations, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VEINNOVATIONS INFILTRATION SYSTEM?

The FDA product code for VEINNOVATIONS INFILTRATION SYSTEM is FRN.

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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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