Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by FLEXICATH LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K063363
11/07/2006
FIRMGRIP PERIPHERALLY INSERTED CATHETER DEVICE
FLEXICATH LTD.
K080793
03/20/2008
FIRMGRIP
FLEXICATH LTD.
K111939
07/08/2011
M/29TM - PRESSURE INJECTABLE
FLEXICATH LTD.
K092629
08/27/2009
SNM FIRMGRIP
FLEXICATH LTD.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact