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FDA 510(k)

MODEL 3875 1 X 8 SC TEST STIMULATION LEAD

K-Number: K062041 · 2006-08-16

ApplicantMedtronic, Inc.
Decision Date2006-08-16
Product CodeGZB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL 3875 1 X 8 SC TEST STIMULATION LEAD is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2006-08-16 under 510(k) number K062041. 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 3875 1 X 8 SC TEST STIMULATION LEAD?

MODEL 3875 1 X 8 SC TEST STIMULATION LEAD is a medical device that received FDA 510(k) clearance on 2006-08-16. The listed applicant is Medtronic, Inc.. The 510(k) number is K062041.

When did MODEL 3875 1 X 8 SC TEST STIMULATION LEAD receive FDA 510(k) clearance?

MODEL 3875 1 X 8 SC TEST STIMULATION LEAD received FDA 510(k) clearance on 2006-08-16, under 510(k) number K062041.

Who is the listed applicant for MODEL 3875 1 X 8 SC TEST STIMULATION LEAD?

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

What is the FDA product code for MODEL 3875 1 X 8 SC TEST STIMULATION LEAD?

The FDA product code for MODEL 3875 1 X 8 SC TEST STIMULATION LEAD is GZB.

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Related Devices (Code: GZB)

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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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