Fehling-Punches— 510(k) K153243

Name: FDA 510(k) clearance K153243
Creator: U.S. Food and Drug Administration
Published: 2016-08-04

Substantially Equivalent

Fehling Instruments GmbH & Co. KG

FDA 510(k) clearance K153243 for Fehling-Punches, Substantially Equivalent on 2016-08-04. Applicant: Fehling Instruments GmbH & Co. KG. Device class: 2.

Clearance details

Applicant: Fehling Instruments GmbH & Co. KG
Product code: Code HAE
Device class: Class 2
Regulation: 21 CFR 882.4840
Advisory panel: Neurology
Date received: 2015-11-09
Decision date: 2016-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Karlstein, DE

Download summary PDF View on FDA.gov ↗

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