Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by David D Cox
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070238
01/25/2007
AMPLATZER RELIANT CATHETER DELIVERY SYSTEM
AGA MEDICAL CORP.
K060400
02/15/2006
CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 68000; CARDIOBLATE BP2 SURGICAL ABLATION DEVICE, MODEL 60831; CARDIOBLAT
MEDTRONIC INC.
K081082
04/16/2008
U-CLIP UNI-FIRE, MODEL M65
MEDTRONIC INC.
K062057
07/20/2006
U-CLIP DEVICE, MODEL NC65
MEDTRONIC VASCULAR
K053252
11/21/2005
U-CLIP DEVICE, MODELS B140, B160 AND B180
MEDTRONIC VASCULAR
K043291
11/29/2004
CARDIOBLATE DISPERSIVE ELECTRODE ADAPTER (ACCESSORY), MODEL 60884
MEDTRONIC VASCULAR
K153690
12/23/2015
PriMatrix Dermal Repair Scaffold
TEI BioSciences Inc.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact