Therakos CELLEX Procedural Kit
FDA premarket approval P860003/S094 · decided 2017-08-18
Approval details
- PMA number
- P860003
- Supplement
- S094
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Therakos CELLEX Procedural Kit
- Generic name
- System, photopheresis, extracorporeal
- Applicant
- Therakos Development Limited
- Date received
- 2017-07-24
- Decision date
- 2017-08-18
- Days to decision
- 25 days
- Decision code
- OK30
- Product code
- LNR
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Dublin
- Statement
- Addition of a new mold tool for the CELLEX Procedural Kit.
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