FDA 510(k)

MODEL 3587A RESUME EPIDURAL LEAD

K-Number: K884948 · 1989-01-17

Decision Date1989-01-17

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MODEL 3587A RESUME EPIDURAL 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 1989-01-17 under 510(k) number K884948. 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 3587A RESUME EPIDURAL LEAD?

MODEL 3587A RESUME EPIDURAL LEAD is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is Medtronic Vascular. The 510(k) number is K884948.

When did MODEL 3587A RESUME EPIDURAL LEAD receive FDA 510(k) clearance?

MODEL 3587A RESUME EPIDURAL LEAD received FDA 510(k) clearance on 1989-01-17, under 510(k) number K884948.

Who is the listed applicant for MODEL 3587A RESUME EPIDURAL 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 MODEL 3587A RESUME EPIDURAL LEAD?

The FDA product code for MODEL 3587A RESUME EPIDURAL 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.