LMT NOMAG IC 3.0— 510(k) K062052

Name: FDA 510(k) clearance K062052
Creator: U.S. Food and Drug Administration
Published: 2006-07-31

Substantially Equivalent

Lmt Lammers Medical Technology GmbH

FDA 510(k) clearance K062052 for LMT NOMAG IC 3.0, Substantially Equivalent on 2006-07-31. Applicant: Lmt Lammers Medical Technology GmbH. Device class: 2.

Clearance details

Applicant: Lmt Lammers Medical Technology GmbH
Product code: Code FPL
Device class: Class 2
Regulation: 21 CFR 880.5410
Advisory panel: General Hospital
Date received: 2006-07-20
Decision date: 2006-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Luebeck, DE

Download summary PDF View on FDA.gov ↗

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