Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by TRUDY ESTRIDGE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070610
03/05/2007
SKATER BILIARY CATHETER
ANGIOTECH
DEN090007
04/17/2009
BIO-SEAL LUNG BIOPSY TRACT SYSTEM
ANGIOTECH
K073672
12/27/2007
SKATER BILIARY CATHETER
ANGIOTECH
K080680
03/10/2008
QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF PDO (POLYDIOXANONE
SURGICAL SPECIALTIES CORP.
K080985
04/07/2008
QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF POLYDIOXANONE (PDO)
SURGICAL SPECIALTIES CORP.
K101832
07/01/2010
BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT
MEDICAL DEVICE TECHNOLOGIES, INC.
K073520
12/14/2007
ANGIOTECH CVC
ANGIOTECH PHARMACEUTICALS, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact