FDA 510(k)

BIFURCATED Y-EXTENSION

K-Number: K953742 · 1996-11-19

Decision Date1996-11-19

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

BIFURCATED Y-EXTENSION is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1996-11-19 under 510(k) number K953742. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIFURCATED Y-EXTENSION?

BIFURCATED Y-EXTENSION is a medical device that received FDA 510(k) clearance on 1996-11-19. The listed applicant is Medtronic Vascular. The 510(k) number is K953742.

When did BIFURCATED Y-EXTENSION receive FDA 510(k) clearance?

BIFURCATED Y-EXTENSION received FDA 510(k) clearance on 1996-11-19, under 510(k) number K953742.

Who is the listed applicant for BIFURCATED Y-EXTENSION?

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

What is the FDA product code for BIFURCATED Y-EXTENSION?

The FDA product code for BIFURCATED Y-EXTENSION is GZB.

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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.