PMA P860003S056
- Device
- CELLEX PROCEDURAL KIT
- Applicant
- Therakos Development Limited
- PMA number
- P860003
- Supplement
- S056
- Product code
- LNR
- Decision date
- 2010-12-09
- Classification
- System, Photopheresis, Extracorporeal
- Generic name
- System, photopheresis, extracorporeal
- Approval order statement
- CHANGE TO A COMPONENT MANUFACTURING PROCEDURE AND A CHANGE TO A TEST METHOD.
Current openFDA PMA Record#
- Device
- CELLEX PROCEDURAL KIT
- Applicant
- Therakos Development Limited
- PMA number
- P860003
- Supplement
- S056
- Product code
- LNR
- Generic name
- System, photopheresis, extracorporeal
- Decision date
- 2010-12-09
- Decision code
- OK30
- Date received
- 2010-11-12
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE TO A COMPONENT MANUFACTURING PROCEDURE AND A CHANGE TO A TEST METHOD.