MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR— 510(k) K884032

Name: FDA 510(k) clearance K884032
Creator: U.S. Food and Drug Administration
Published: 1988-10-13

Substantially Equivalent

Morgan Associates, Inc.

FDA 510(k) clearance K884032 for MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, Substantially Equivalent on 1988-10-13. Applicant: Morgan Associates, Inc.. Device class: 2.

Clearance details

Applicant: Morgan Associates, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1988-09-23
Decision date: 1988-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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