THERAKOS CELLEX PHOTOPHERESIS SYSTEM PROCEDURAL KIT
FDA premarket approval P860003/S059 · decided 2011-05-13
Approval details
- PMA number
- P860003
- Supplement
- S059
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- THERAKOS CELLEX PHOTOPHERESIS SYSTEM PROCEDURAL KIT
- Generic name
- System, photopheresis, extracorporeal
- Applicant
- Therakos Development Limited
- Date received
- 2011-03-14
- Decision date
- 2011-05-13
- Days to decision
- 60 days
- Decision code
- APPR
- Product code
- LNR
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Dublin
- Statement
- APPROVAL FOR A MINOR DIMENSIONAL CHANGE TO A Y-ADAPTOR IN THE CELLEX PROCEDURAL KIT AND A CHANGE IN THE SPLICE BOND BUSHING OF THE CELLEX PROCEDURAL KITS ANTICOAGULANT (GREEN) LINE.
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