FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

E.G. SCAN II ESPHAGOSCOPE SYSTEM

K Number: K120702 · Decision Jun 20, 2012
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
29
Applicant Total
11
Review Days
104

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Basic Information

Device Name
E.G. SCAN II ESPHAGOSCOPE SYSTEM
K Number
K120702
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4710
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intromedic Co., Ltd.
Date Received
March 8, 2012
Decision Date
June 20, 2012
Product Code
EOX
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EOX Esophagoscope (Flexible Or Rigid)

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Other Clearances by Intromedic Co., Ltd.

K Number Device Name
K252617 MiroCam® Capsule Endoscope System
K180732 MiroCam Capsule Endoscope System
K170438 MiroCam Capsule Endoscope System
K143663 MiroCam Capsule Endoscope System
K134005 MIROCAM CAPSULE ENDOSCOPE SYSTEM
K140751 MIROCAM CAPSULE ENDOSCOPE SYSTEM
K131131 E.G. SCAN(TM) II ESOPHAGOSCOPE SYSTEM
K123428 MIROCAM CAPSULE ENDOSCOPE SYSTEM
K111450 MIROCAM CAPSULE ENDOSCOPE SYSTEM
K111030 E.G. SCAN (TM) ESOPHAGOSCOPE SYSTEM
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