Cytori Therapeutics, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K113255 | PUREGRAFT 850/PURE SYSTEM | MUU | 2012-03-07 | View |
| 510(k) | K092923 | CYTORI PUREGRAFT 250/PURE SYSTEM | MUU | 2010-01-06 | View |
| 510(k) | K072587 | CYTORI AFT SYSTEM | MUU | 2007-12-10 | View |
| 510(k) | K063235 | CYTORI LIPOPLASTY SYSTEM WITH CELASE REAGENT | QPB | 2007-01-24 | View |
| 510(k) | K060482 | CYTORI CELUTION CELL CONCENTRATION DEVICE | CAC | 2006-09-28 | View |
No matching devices.
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