FDA 510(k)

MEDTRONIC MODEL 7495 EXTENSION KIT

K-Number: K990104 · 1999-02-09

Decision Date1999-02-09

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC MODEL 7495 EXTENSION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1999-02-09 under 510(k) number K990104. 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 MEDTRONIC MODEL 7495 EXTENSION KIT?

MEDTRONIC MODEL 7495 EXTENSION KIT is a medical device that received FDA 510(k) clearance on 1999-02-09. The listed applicant is Medtronic Vascular. The 510(k) number is K990104.

When did MEDTRONIC MODEL 7495 EXTENSION KIT receive FDA 510(k) clearance?

MEDTRONIC MODEL 7495 EXTENSION KIT received FDA 510(k) clearance on 1999-02-09, under 510(k) number K990104.

Who is the listed applicant for MEDTRONIC MODEL 7495 EXTENSION KIT?

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 MEDTRONIC MODEL 7495 EXTENSION KIT?

The FDA product code for MEDTRONIC MODEL 7495 EXTENSION KIT 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.