Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by SHIRLEY HYINK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K132099
07/08/2013
ARTHROCARE COBLATOR IQ DLR SPINEWAND, ARTHROCARE COBLATOR IQ DLG SPINEWAND
ARTHROCARE CORPORATION
K162074
07/27/2016
Werewolf RF20000 Controller, FLOW 50 Wand
ARTHROCARE CORPORATION
K072556
09/10/2007
HEMOSTASIS VALVE
MERIT MEDICAL SYSTEMS, INC.
K073035
10/29/2007
PRELUDE AND PRELUDE PRO SHEATH INTRODUCERS
MERIT MEDICAL SYSTEMS, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact