510(k) K854905

Device
PERCUTANEOUS NEPHROSTOMY SETS (LOOP TECHNIQUE)
Applicant
ANGIOMED U.S., INC.
510(k) number
K854905
Product code
GBO  
Decision
Substantially Equivalent (SESE)
Decision date
1986-01-24
Date received
1985-12-09
Regulation
878.4200
Classification name
Catheter, Nephrostomy, General & Plastic Surgery
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
RICHARD P MOHR
Address
4081 E. La Palma Ave., Suite E Anaheim CA US 92807 92807

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code GBO  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K041995MODIFICATION TO: GP GENERAL PURPOSE DRAINAGE CATHETER, MINI-PIG DRAINAGE CATHETER, NEPHROSTOMY CATHETER, BILIARYUresil, LLC2004-08-19
K021632GP GENERAL PURPOSE DRAINAGE CATHETER; MINI-PIGTAIL DRAINAGE CATHETER WITH LOCKING PIGTAIL; GP GENERAL PURPOSE DRAINAGE CUresil, L.P.2002-06-13
K912109URESIL GENERAL PURPOSE DRAINAGE CATHETERUresil Corp.1991-08-12
K854906PERCUTANEOUS NEPHROSTOMY SETS (OTTO)Angiomed U.S., Inc.1986-01-24
K854907PERCUTANEOUS NEPHROSTOMY SETS (GUNTHER)Angiomed U.S., Inc.1986-01-24
K854909PEDIATRIC PERCUTANEOUS NEPHROSTOMY SETSAngiomed U.S., Inc.1986-01-24
K854911PERCUTANEOUS NEPHROSTOMY SETS (SCHULLER)Angiomed U.S., Inc.1986-01-24
K820867PERCUTANEOUS NEPHROSTOMY SETVan-Tec, Inc.1982-04-13
K781664SILASTIC NEPHROSTOMY SYSTEMDow Corning Corp. Healthcare Industries Materials1979-01-22
K781526SILASTIC U-TUBE KITDow Corning Corp. Healthcare Industries Materials1978-09-20

Legacy Summary#

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FDA Review#

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