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FDA 510(k)

D'Vill Introducer

K-Number: K171206 · 2017-10-20

ApplicantNuMED, Inc.
Decision Date2017-10-20
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

D'Vill Introducer is the device name listed in this FDA 510(k) record. The listed applicant is NuMED, Inc.. It received FDA 510(k) clearance on 2017-10-20 under 510(k) number K171206. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the D'Vill Introducer?

D'Vill Introducer is a medical device that received FDA 510(k) clearance on 2017-10-20. The listed applicant is NuMED, Inc.. The 510(k) number is K171206.

When did D'Vill Introducer receive FDA 510(k) clearance?

D'Vill Introducer received FDA 510(k) clearance on 2017-10-20, under 510(k) number K171206.

Who is the listed applicant for D'Vill Introducer?

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

What is the FDA product code for D'Vill Introducer?

The FDA product code for D'Vill Introducer is DYB.

Other records listing NuMED, 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.

View all 9 devices →

Related Devices (Code: DYB)

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.