ULTRAHESIVE II POSTOP ELECTRODE— 510(k) K862028

Substantially Equivalent

Medical Devices, Inc.

FDA 510(k) clearance K862028 for ULTRAHESIVE II POSTOP ELECTRODE, Substantially Equivalent on 1986-08-01. Applicant: Medical Devices, Inc..

Clearance details

Applicant: Medical Devices, Inc.
Product code: Code GXY
Advisory panel: Neurology
Date received: 1986-05-28
Decision date: 1986-08-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

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