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FDA 510(k)

IMPULSE EPIDURAL ELECTRODE

K-Number: K884663 · 1989-01-17

ApplicantImpulse Systems, Inc.
Decision Date1989-01-17
Product CodeJXE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

IMPULSE EPIDURAL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Impulse Systems, Inc.. It received FDA 510(k) clearance on 1989-01-17 under 510(k) number K884663. The device is classified under product code JXE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPULSE EPIDURAL ELECTRODE?

IMPULSE EPIDURAL ELECTRODE is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is Impulse Systems, Inc.. The 510(k) number is K884663.

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

IMPULSE EPIDURAL ELECTRODE received FDA 510(k) clearance on 1989-01-17, under 510(k) number K884663.

Who is the listed applicant for IMPULSE EPIDURAL ELECTRODE?

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

What is the FDA product code for IMPULSE EPIDURAL ELECTRODE?

The FDA product code for IMPULSE EPIDURAL ELECTRODE is JXE.

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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.

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