TRANSCUTANEOUS ELECTRICAL NERVE STIMULATION— 510(k) K896787

Name: FDA 510(k) clearance K896787
Creator: U.S. Food and Drug Administration
Published: 1990-07-30

Substantially Equivalent

Saratoga Intl., Inc.

FDA 510(k) clearance K896787 for TRANSCUTANEOUS ELECTRICAL NERVE STIMULATION, Substantially Equivalent on 1990-07-30. Applicant: Saratoga Intl., Inc.. Device class: 2.

Clearance details

Applicant: Saratoga Intl., Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1989-12-04
Decision date: 1990-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

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