510(k) K770535

Device: C-DAK 3500
Applicant: Cordis Corp.
510(k) number: K770535
Product code: FIG
Decision: Substantially Equivalent (SESE)
Decision date: 1977-04-15
Date received: 1977-03-21
Regulation: 876.5820
Classification name: Clamp, Tubing, Blood, Automatic
Medical specialty: Gastroenterology, Urology
Review panel: Gastroenterology, Urology
Device class: 2
Clearance type: Traditional
Third party reviewed: N

Applicant Contact#

Address: 803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

1220973

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FIG#

510(k), Device, Applicant table
510(k)	Device	Applicant	Decision date
K093915	DEKA TAC DEVICE	Deka Research & Development Corp.	2011-08-23
K921993	ELS AUTOMATIC TUBING CLAMP SYSTEM	Rocky Mountain Research, Inc.	1994-01-05
K914459	AUTOMATIC TUBING CLAMP	Rocky Mountain Research, Inc.	1992-06-24