FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

E.G. SCAN(TM) II ESOPHAGOSCOPE SYSTEM

K Number: K131131 · Decision Jun 21, 2013
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
29
Applicant Total
11
Review Days
60

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Basic Information

Device Name
E.G. SCAN(TM) II ESOPHAGOSCOPE SYSTEM
K Number
K131131
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
874.4710
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intromedic Co., Ltd.
Date Received
April 22, 2013
Decision Date
June 21, 2013
Product Code
EOX
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

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)

Similar 510(k) Clearances

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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
K123428 MIROCAM CAPSULE ENDOSCOPE SYSTEM
K120702 E.G. SCAN II ESPHAGOSCOPE SYSTEM
K111450 MIROCAM CAPSULE ENDOSCOPE SYSTEM
K111030 E.G. SCAN (TM) ESOPHAGOSCOPE SYSTEM
Search all 11 clearances from Intromedic Co., Ltd. →