IMPULSE EPIDURAL ELECTRODE— 510(k) K884663

Name: FDA 510(k) clearance K884663
Creator: U.S. Food and Drug Administration
Published: 1989-01-17

Substantially Equivalent

Impulse Systems, Inc.

FDA 510(k) clearance K884663 for IMPULSE EPIDURAL ELECTRODE, Substantially Equivalent on 1989-01-17. Applicant: Impulse Systems, Inc.. Device class: 2.

Clearance details

Applicant: Impulse Systems, Inc.
Product code: Code JXE
Device class: Class 2
Regulation: 21 CFR 882.1550
Advisory panel: Neurology
Date received: 1988-11-07
Decision date: 1989-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, WI, US

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