This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Replacement of the annealing oven used in the manufacturing process of the hollow fibers for the plasmaflo device.
| Device | Plasmaflo |
| Classification Name | Separator For Therapeutic Purposes, Membrane Automated Blood Cell/plasma |
| Generic Name | Separator For Therapeutic Purposes, Membrane Automated Blood Cell/plasma |
| Applicant | Asahi Kasei Medical Co., Ltd. |
| Date Received | 2017-12-20 |
| Decision Date | 2018-01-17 |
| PMA | P820033 |
| Supplement | S011 |
| Product Code | MDP |
| Docket Number | Premarket Approval (PMA) // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices Radia |
| Advisory Committee | Gastroenterology/Urology |
| Supplement Type | 30-day Notice |
| Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | Asahi Kasei Medical Co., Ltd. 1-105 Kanda Jinbocho chiyoda-ku tokyo 101-8-8101 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P820033 | Original Filing | |
| S016 | 2022-12-09 | 30-day Notice |
| S015 | 2022-01-11 | 30-day Notice |
| S014 | 2021-02-01 | 30-day Notice |
| S013 | 2020-09-24 | 30-day Notice |
| S012 | 2018-01-19 | 30-day Notice |
| S011 | 2017-12-20 | 30-day Notice |
| S010 | 2016-02-19 | 30-day Notice |
| S009 | 2015-11-06 | 30-day Notice |
| S008 | 2011-10-12 | 30-day Notice |
| S007 | 2010-12-15 | 30-day Notice |
| S006 | 2010-07-07 | 30-day Notice |
| S005 | 2009-08-18 | Normal 180 Day Track |
| S004 | ||
| S003 | ||
| S002 | ||
| S001 | 1984-04-20 |