Endoscopic Spine System 510(k) FDA Premarket Notification ... | 合法醫療器材資訊網
Arthroscope
ARTHRO KINETICS INC.
FDA.report
[1]
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PMN
[2]
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ARTHRO KINETICS
INC.
[3]
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K061246
[4]
The following data is part of a premarket notification filed by Arthro Kinetics Inc. with the FDA for Endoscopic Spine System.
Pre-market Notification Details Device ID K061246 510k Number K061246 Device Name: ENDOSCOPIC SPINE SYSTEM Classification Arthroscope ...
"Arthro Kinetics"Endoscopic Spinal System "Arthro Kinetics"Endoscopic Spinal System FeNO No breath Autonio Foundation "Chrisofix"splint(Non-Sterile) 錶式血壓計價格 手 壓 式血壓計 “康/”醫療用活性碳平面口罩 (未滅菌) How to calculate hdl from total
"艾梭肯尼特"脊椎內視鏡系統"Arthro Kinetics"Endoscopic ... | 合法醫療器材資訊網
"艾梭肯尼特"脊椎內視鏡系統"Arthro Kinetics"Endoscopic Spinal ... | 合法醫療器材資訊網
510(k) Summary for Arthro Kinetics Endoscopic Spine System | 合法醫療器材資訊網
Endoscopic Spine System 510(k) FDA Premarket Notification ... | 合法醫療器材資訊網
Arthro Kinetics Inc FDA Filings | 合法醫療器材資訊網
【”艾梭肯尼特”脊椎內視鏡系統】許可證字號 | 合法醫療器材資訊網
Section 1.0 510(k) Summary | 合法醫療器材資訊網
K12261JAN 510(k) | 合法醫療器材資訊網
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