FDA 510(k)

MODEL NOS. 7495 AND 501826 EXTENSIONS

K-Number: K954886 · 1995-11-27

Decision Date1995-11-27

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MODEL NOS. 7495 AND 501826 EXTENSIONS is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1995-11-27 under 510(k) number K954886. 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 MODEL NOS. 7495 AND 501826 EXTENSIONS?

MODEL NOS. 7495 AND 501826 EXTENSIONS is a medical device that received FDA 510(k) clearance on 1995-11-27. The listed applicant is Medtronic Vascular. The 510(k) number is K954886.

When did MODEL NOS. 7495 AND 501826 EXTENSIONS receive FDA 510(k) clearance?

MODEL NOS. 7495 AND 501826 EXTENSIONS received FDA 510(k) clearance on 1995-11-27, under 510(k) number K954886.

Who is the listed applicant for MODEL NOS. 7495 AND 501826 EXTENSIONS?

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 MODEL NOS. 7495 AND 501826 EXTENSIONS?

The FDA product code for MODEL NOS. 7495 AND 501826 EXTENSIONS 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.