FDA 510(k)

NICOLET EPIDURAL SPINAL ELECTRODE

K-Number: K882053 · 1988-10-18

Decision Date1988-10-18

Product CodeGYC

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

NICOLET EPIDURAL SPINAL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Nicolet Instrument Corp.. It received FDA 510(k) clearance on 1988-10-18 under 510(k) number K882053. The device is classified under product code GYC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NICOLET EPIDURAL SPINAL ELECTRODE?

NICOLET EPIDURAL SPINAL ELECTRODE is a medical device that received FDA 510(k) clearance on 1988-10-18. The listed applicant is Nicolet Instrument Corp.. The 510(k) number is K882053.

When did NICOLET EPIDURAL SPINAL ELECTRODE receive FDA 510(k) clearance?

NICOLET EPIDURAL SPINAL ELECTRODE received FDA 510(k) clearance on 1988-10-18, under 510(k) number K882053.

Who is the listed applicant for NICOLET EPIDURAL SPINAL ELECTRODE?

The FDA 510(k) record lists Nicolet Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NICOLET EPIDURAL SPINAL ELECTRODE?

The FDA product code for NICOLET EPIDURAL SPINAL ELECTRODE is GYC.

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Other records listing Nicolet Instrument Corp. as applicant

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Related Devices (Code: GYC)

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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.