Gambro Prismaflex TPE 2000 Set
FDA premarket approval P830063/S028 · decided 2024-10-24
Approval details
- PMA number
- P830063
- Supplement
- S028
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Gambro Prismaflex TPE 2000 Set
- Generic name
- Separator for therapeutic purposes, membrane automated blood cell/plasma
- Applicant
- Vantive US Healthcare, LLC
- Date received
- 2024-09-26
- Decision date
- 2024-10-24
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- MDP
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Deerfield, IL
- Statement
- approval for change from manual production equipment to automated production equipment used to place the Tyvek window on the primary packaging bag (pouch) of the Gambro Prismaflex TPE 2000 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 |