Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by CATHETER LLC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030538
02/20/2003
AMERICAN CATHETER, MODEL W3
CATHETER LLC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact