510(k) K111030

Device
E.G. SCAN (TM) ESOPHAGOSCOPE SYSTEM
Applicant
INTROMEDIC CO., LTD
510(k) number
K111030
Product code
EOX  
Decision
Substantially Equivalent (SESE)
Decision date
2011-10-21
Date received
2011-04-13
Regulation
874.4710
Classification name
Esophagoscope (flexible Or Rigid)
Medical specialty
Ear Nose & Throat
Review panel
Ear Nose & Throat
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
Yes

Applicant Contact#

Contact
JINYOUNG LEE
Address
Suite 1104 E&C Venture Dream Tower 6-Cha, 197-28 Guro-Dong Guro-Gu , Seoul KR 152719 152719

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code EOX  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K233142EndoSign® Cell collection device (ES-CYT-102)Cyted Limited2024-01-19
K230339EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.2023-02-24
K223072PENTAX Medical Video Esophagoscope EE17-J10Pentax of America, Inc.2022-12-02
K222366EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.2022-10-26
K203450EsophaCap Swallowable Cellular Retrieval Device (changed from Cell-Mata)Capnostics, LLC2021-05-04
K210137EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.2021-02-18
K192523CMOS Video Esophagoscope SSUKarl Storz SE & CO. KG2020-01-24
K183262EsoCheck CCD Cell Collection DeviceLucid Diagnostics, Inc.2019-06-21
K182159Strome-Blitzer Cytology BalloonAdn International, LLC2019-06-13
K181292PrimeSight™ UNITY 9000 Video Processor, PrimeSight™ UNITY 9100 Video ProcessorCogentix Medical, Inc.2018-11-15
K181020Cytosponge Cell Collection DeviceCovidien, LLC2018-08-16
K152794Cytosponge Cell Collection DeviceCovidien, LLC2016-04-12
K142695Cytosponge Cell Collection DeviceCovidien, LLC2014-11-26
K131131E.G. SCAN(TM) II ESOPHAGOSCOPE SYSTEMIntromedic Co., Ltd.2013-06-21
K120702E.G. SCAN II ESPHAGOSCOPE SYSTEMIntromedic Co., Ltd.2012-06-20

Legacy Summary#

summary

FDA Review#

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