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FDA 510(k)

FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFT

K-Number: K050832 · 2005-07-07

ApplicantBard Peripheral Vascular, Inc.
Decision Date2005-07-07
Product CodeJCT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFT is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2005-07-07 under 510(k) number K050832. The device is classified under product code JCT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFT?

FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFT is a medical device that received FDA 510(k) clearance on 2005-07-07. The listed applicant is Bard Peripheral Vascular, Inc.. The 510(k) number is K050832.

When did FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFT receive FDA 510(k) clearance?

FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFT received FDA 510(k) clearance on 2005-07-07, under 510(k) number K050832.

Who is the listed applicant for FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFT?

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

What is the FDA product code for FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFT?

The FDA product code for FLUENCY PLUS TRACHEOBRONCHIAL STENT GRAFT is JCT.

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Related Devices (Code: JCT)

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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Official Source

View on FDA Database →

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

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