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FDA 510(k)

MEDUSA VASCULAR PLUG

K-Number: K123696 · 2013-10-25

ApplicantEndoshape, Inc.
Decision Date2013-10-25
Product CodeKRD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDUSA VASCULAR PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Endoshape, Inc.. It received FDA 510(k) clearance on 2013-10-25 under 510(k) number K123696. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDUSA VASCULAR PLUG?

MEDUSA VASCULAR PLUG is a medical device that received FDA 510(k) clearance on 2013-10-25. The listed applicant is Endoshape, Inc.. The 510(k) number is K123696.

When did MEDUSA VASCULAR PLUG receive FDA 510(k) clearance?

MEDUSA VASCULAR PLUG received FDA 510(k) clearance on 2013-10-25, under 510(k) number K123696.

Who is the listed applicant for MEDUSA VASCULAR PLUG?

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

What is the FDA product code for MEDUSA VASCULAR PLUG?

The FDA product code for MEDUSA VASCULAR PLUG is KRD.

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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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