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FDA 510(k)

CONVOY ADVANCED DELIVERY SHEATH

K-Number: K072719 · 2008-03-07

Decision Date2008-03-07
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONVOY ADVANCED DELIVERY SHEATH is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2008-03-07 under 510(k) number K072719. 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 CONVOY ADVANCED DELIVERY SHEATH?

CONVOY ADVANCED DELIVERY SHEATH is a medical device that received FDA 510(k) clearance on 2008-03-07. The listed applicant is Boston Scientific Corp. The 510(k) number is K072719.

When did CONVOY ADVANCED DELIVERY SHEATH receive FDA 510(k) clearance?

CONVOY ADVANCED DELIVERY SHEATH received FDA 510(k) clearance on 2008-03-07, under 510(k) number K072719.

Who is the listed applicant for CONVOY ADVANCED DELIVERY SHEATH?

The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVOY ADVANCED DELIVERY SHEATH?

The FDA product code for CONVOY ADVANCED DELIVERY SHEATH is DYB.

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 Boston Scientific Corp 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: 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.

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