Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by POLYSTAN A/S
FDA 510(k) Number
Submission Date
Device Name
Applicant
K022281
07/15/2002
SAFE MAXI VENOUS/CARDIOTOMY RESERVIOR, MODEL 016045
POLYSTAN A/S
K013038
09/10/2001
SAFE MAXI HOLLOW FIBER OXYGENATOR, MODEL 016010
POLYSTAN A/S
K023251
09/30/2002
PEDIATRIC ARTERIAL CANNULA
POLYSTAN A/S
K953976
08/23/1995
SAFE MICRO
POLYSTAN A/S
K980974
03/16/1998
SAFE MINI
POLYSTAN A/S
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact