Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by REGINA YEH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020089
01/10/2002
MAHURKAR TRIPLE LUMEN CATHETER, 12 FR
THE KENDALL COMPANY
K000087
01/12/2000
MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR
THE KENDAL CO.
K030209
01/21/2003
MAHURKAR OPLUS CATHETER, MODEL 13.5 FR
THE KENDALL COMPANY
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact