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FDA 510(k) & PMA Approved Devices — 13 products

Total Devices13
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K874027 LIPASE UV [TOYO]CHI1988-05-27 View
510(k) K873792 SEPACELL R-500 AND SEPACELL R-500ACAK1988-01-19 View
510(k) K855251 MODIFICATION ASAHI NEW PAN-SERIES HEMOFILTERSKDI1986-02-04 View
510(k) K855212 ASAHI AM SERIES DIALYZERSFJI1986-01-21 View
510(k) K854259 SEPACELL R-500 & SEPACELL R-500ACAK1986-01-08 View
510(k) K842103 TOYO JOZO URIC ACID TESTKNK1984-08-12 View
510(k) K842104 TOYO JOZO G-GTP TESTJPZ1984-08-10 View
510(k) K830231 ASAHI HOLLOW FIBER KIDNEYS, AM-SERIESKOC1983-03-17 View
510(k) K830183 ASAHI HOLLOW FIBER KIDNEYS NR SERIESKOC1983-03-17 View
510(k) K823733 EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIRKOC1983-01-14 View
510(k) K813037 FLOWGUARD CATHETERS & CANNALAEDWF1981-12-14 View
510(k) K813035 POLYSTAN VERTICLUDE BLOOD PUMPDWB1981-11-27 View
510(k) K813034 POLYSTAN HEART LUNG MACHINE SYSDTQ1981-11-27 View
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