FDA 510(k)

MEDTRONIC MODEL 3888 PISCES-QUAD PLUS LEAD

K-Number: K923567 · 1992-11-05

Decision Date1992-11-05

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC MODEL 3888 PISCES-QUAD PLUS LEAD is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1992-11-05 under 510(k) number K923567. 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 3888 PISCES-QUAD PLUS LEAD?

MEDTRONIC MODEL 3888 PISCES-QUAD PLUS LEAD is a medical device that received FDA 510(k) clearance on 1992-11-05. The listed applicant is Medtronic Vascular. The 510(k) number is K923567.

When did MEDTRONIC MODEL 3888 PISCES-QUAD PLUS LEAD receive FDA 510(k) clearance?

MEDTRONIC MODEL 3888 PISCES-QUAD PLUS LEAD received FDA 510(k) clearance on 1992-11-05, under 510(k) number K923567.

Who is the listed applicant for MEDTRONIC MODEL 3888 PISCES-QUAD PLUS LEAD?

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 3888 PISCES-QUAD PLUS LEAD?

The FDA product code for MEDTRONIC MODEL 3888 PISCES-QUAD PLUS LEAD 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.