Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by CASEY COOMBS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K162900
10/17/2016
PowerMidline Catheter
C.R. Bard, Inc.
K153280
11/12/2015
PowerGlide Pro Midline Catheter
C.R. BARD, INC.
K153298
11/13/2015
AccuCath Intravascular Catheter
C.R. Bard, Inc.
K153393
11/24/2015
PowerMidline Catheter
C.R. BARD, INC
K133856
12/19/2013
POWERGLIDE MIDLINE CATHETER
C.R. BARD, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact