Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by DEBBIE KIDDER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070311
02/01/2007
CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261
MEDTRONIC VASCULAR
K170524
02/22/2017
Access AMH
Beckman Coulter, Inc.
K082475
08/28/2008
REVEAL XT INSERTABLE CARDIAC MONITOR, MODEL 9529, REVEL DX INSERTABLE CARDIAC MONITOR, MODEL 9528
MEDTRONIC INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact