510(k) K905154

Device
GASTROSCAN
Applicant
MEDICS INSTRUMENT CORP.
510(k) number
K905154
Product code
FFX  
Decision
Substantially Equivalent (SESE)
Decision date
1991-06-19
Date received
1990-11-15
Regulation
876.1725
Classification name
System, Gastrointestinal Motility (electrical)
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
JOHN MATHERLY
Address
Friedhofplatz 16, Pob 706 Ch-4502 Solothurn, Switzerland SE

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FFX  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K252605mcompass Anorectal Balloon Expulsion Catheter (RMD-003-001)Medspira, LLC2025-12-05
K240007Solar Compact (G4-1)Laborie Medical Technologies, Corp.2024-05-06
K231861EndoflipTM 300 SystemCovidien, LLC2023-07-21
K223705EndoflipTM 300Covidien, LLC2023-04-14
K222000Transit-PelletsMedifactia AB2023-01-18
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#

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FDA Review#

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