510(k) K102801

Device
PHTIP DISPOSABLE ISFET CATHETER
Applicant
E-CATH CO., LTD
510(k) number
K102801
Product code
FFX  
Decision
Substantially Equivalent (SESE)
Decision date
2010-10-26
Date received
2010-09-27
Regulation
876.1725
Classification name
System, Gastrointestinal Motility (electrical)
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
ROBERT N CLARK
Address
13605 W. 7th Ave. Golden CO US 80401 80401

FDA Registration Numbers

Source Documents

510(k) summary PDF

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K201106IntraMarX 3D Radiopaque MarkerAnx Robotica Corp2020-05-21
K191087IntraMarX Radiopaque MarkersAnx Robotica Corp2019-12-18
K190208Diversatek Healthcare High Resolution Impedance Manometry (HRiM) ProbeDiversatek Healthcare2019-10-03
K181760Transit-PelletsMedifactia AB2019-08-08
K183072EndoFLIP SystemCrospon, Ltd.2019-02-15
K181750SITZMARKSKonsyl Pharmaceuticals2018-11-15
K170833EndoFLIP® System with FLIP Topography moduleCrospon, Ltd.2017-04-17
K160287Rapid Barostat Bag (RBB) Pump and CatheterMui Scientific2017-03-14
K160170Lehman Manometry CatheterWilson-Cook Medical, Inc.2016-06-20
K160725EndoFLIPCrospon, Ltd.2016-05-01

Legacy Summary

summary

FDA Review

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