510(k) K993738

Device
DISPOS-A-SCOPE
Applicant
DISPOS-A-SCOPE
510(k) number
K993738
Product code
FER  
Decision
Substantially Equivalent (SESE)
Decision date
2000-01-06
Date received
1999-11-04
Regulation
876.1500
Classification name
Anoscope And Accessories
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
LAUREL NICHOLAS
Address
315 Skyline Dr. Lewiston ID US 83501 83501

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code FER  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K250645SleeveLUX 24 Anoscope/Proctoscope (P2001); SleeveLUX 16 Anoscope/Proctoscope (P2002)Haemoband Surgical, Ltd.2025-10-09
K242668Gastro Concepts Air AssistGastro Concepts, LLC2024-12-13
K230439WellCare AnoscopeWell Care (Wuhan) Medical Technology Co., Ltd.2023-12-22
K200021Applied Medical AnoscopeApplied Medical Resources2021-01-06
K171701GelPOINT Path Transanal Access PlatformApplied Medical Resources Corp.2017-07-20
K133393GELPOINT PATH TRANSANAL ACCESS PLATFORMApplied Medical Resources Corp.2014-01-02
K133687THD N-ANO ANOSCOPEThd Spa2013-12-11
K121604ANOSPEC DISPOSABLE ANSOSCOPE WITH LIGHTObp Corporation2012-07-27
K121135THD ANOSCOPE, PROCTOSCOPE, RECTOSCOPE, RECTOSCOPE AND LIGHT-SCOPEThd Spa2012-06-01
K110792GELPOINT PATHApplied Medical Resources Corp.2011-05-23
K103647THD DISPOSABLE ANOSCOPES, PROCTOSCOPES AND RECTOSCOPESThd Spa2011-03-01
K093896ETHICON ENDO SURGERY SLOTTED ANOSCOPEEthicon Endo-Surgery, Inc.2010-03-25
K091490FAMILY OF THD DISPOSABLE ANOSCOPES/PROCTOSCOPES/RECTOSCOPESThd Spa2009-06-11
K090432HEMORPEX SYSTEMAngiologica B. M. Srl2009-05-29
K080132THD DISPOSABLE ANOSCOPE/PROCTOSCOPEThd Spa2008-04-09

Legacy Summary#

summary

FDA Review#

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