Tek RMD (Tek Robotic Mobilization Device)— 510(k) K150548

Name: FDA 510(k) clearance K150548
Creator: U.S. Food and Drug Administration
Published: 2015-06-11

Substantially Equivalent

Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S

FDA 510(k) clearance K150548 for Tek RMD (Tek Robotic Mobilization Device), Substantially Equivalent on 2015-06-11. Applicant: Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S. Device class: 2.

Clearance details

Applicant: Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S
Product code: Code IPL
Device class: Class 2
Regulation: 21 CFR 890.3900
Advisory panel: Physical Medicine
Date received: 2015-03-03
Decision date: 2015-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Istanbul, TR

Download summary PDF View on FDA.gov ↗

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