Prismaflex TPE2000 Set
FDA premarket approval P830063/S027 · decided 2024-01-10
Approval details
- PMA number
- P830063
- Supplement
- S027
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Prismaflex TPE2000 Set
- Generic name
- Separator for therapeutic purposes, membrane automated blood cell/plasma
- Applicant
- Vantive US Healthcare, LLC
- Date received
- 2023-12-15
- Decision date
- 2024-01-10
- Days to decision
- 26 days
- Decision code
- OK30
- Product code
- MDP
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Deerfield, IL
- Statement
- the transfer of manufacturing site for components of the Prismaflex TPE2000 Set and a manufacturing process change for the removal of a superfluous air flow test ofthe Prismaflex TPE2000 Set
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| AK 98 Dialysis Machine (955607) (K250508) | Vantive US Healthcare, LLC | 2025-08-01 |