ETG 255 COMBO STIMUALTOR, TEN 260 STIMUALTOR— 510(k) K110390

Name: FDA 510(k) clearance K110390
Creator: U.S. Food and Drug Administration
Published: 2011-07-29

Substantially Equivalent

Handelshaus Dittman GmbH

FDA 510(k) clearance K110390 for ETG 255 COMBO STIMUALTOR, TEN 260 STIMUALTOR, Substantially Equivalent on 2011-07-29. Applicant: Handelshaus Dittman GmbH. Device class: 2.

Clearance details

Applicant: Handelshaus Dittman GmbH
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2011-02-11
Decision date: 2011-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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