510(k) K885167

Device
TRUDELL BENT CATHETER
Applicant
SIL-MED CORP.
510(k) number
K885167
Product code
FJS  
Decision
Substantially Equivalent (SESE)
Decision date
1989-01-31
Date received
1988-12-13
Regulation
876.5630
Classification name
Catheter, Peritoneal, Long-term Indwelling
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
S MCCALLUM
Address
700 Warner Blvd. Taunton MA US 02780 02780

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FJS  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K213602Argyle Peritoneal Dialysis Cathetor and Kit, Ritus Peritoneal Dialysis Catheter Tunneling Tool KitCovidien, LLC2022-01-14
K180485Argyle Peritoneal Dialysis Catheter and Kits, Argyle Presternal Peritoneal Dialysis Catheter and Kits, Argyle Peritoneal Dialysis Accessory Two Part Titanium Luer Adapter, Argyle Adult Peritoneal Dialysis Accessory Titanium Catheter ExtenderCovidien, LLC2018-07-27
K130441FALLER STYLETMedionics International, Inc.2013-04-19
K121383PS X SERIES (BASIC COMPONENTS AND CATHETER), PD X SERIES (CATHETER WITH ALL COMPONENTS)Medical Components, Inc.2012-09-05
K120130FALLER TROCARMedigroup, Inc.2012-05-21
K113354VETA PERITONEAL DIALYSIS CATHETERPfm Medical, Inc.2012-03-13
K071167FLEX-NECK EXXTENDED PERITONEAL DIALYSIS CATHETER AND ACCESSORIES, MODEL CF-5560Medigroup, Inc.2007-08-31
K070730FLEX-NECK ARC CATHETERMedigroup, Inc.2007-07-03
K060897EMBEDDING TOOL, MODEL TE-1000Medigroup, Inc.2006-07-18
K053123PD CATHMed-Conduit, Inc.2006-03-29
K031351FLEX-NECK PD CATHETER, INFANTMedigroup, Inc.2003-09-17
K012502MEDIGROUP CATHETER EXTENDER/REPAIR KITJanin Group, Inc.2002-02-04
K013017MEDIGROUP KEY TUBEJanin Group, Inc.2001-12-06
K993149PERITONEAL DIALYSIS CATHETERS AND ADAPTERSMedionics International, Inc.2000-04-28
K991042ASH ADVANTAGE PERITONEAL CATHETERJanin Group, Inc.1999-06-25

Legacy Summary#

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FDA Review#

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