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Schiff & Co.

FDA 510(k) & PMA Approved Devices — 15 products

Total Devices15
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K990511 X-TIP INTRAOSSEOUS PERFORATORDZM1999-04-27 View
510(k) K982136 JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200DTN1999-03-24 View
510(k) K981629 NUTRISAFE ENTERAL FEEDING TUBEFPD1999-02-04 View
510(k) K981630 VYGON DOUBLE LUMEN UMBILICAL CATHETERFOS1998-10-01 View
510(k) K974141 PLUS REUSABLE RESUSCITATORBTM1998-05-21 View
510(k) K954448 VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEMFRA1996-10-28 View
510(k) K955085 HM-CAP EIA TEST (MODIFICATION)LYR1996-02-09 View
510(k) K944159 HM-CAP EIA KITLYR1995-07-18 View
510(k) K943521 VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTUREFRA1995-02-14 View
510(k) K896684 KEMBLE LIQUID HANDLING SYSTEM DISPENSERJQW1990-04-16 View
510(k) K894617 OLYMPUS PK-TP SYSTEM REACTIVE CONTROLGMI1989-10-31 View
510(k) K895967 FASTEC 901 AGGLUTINATION PATTERN READERJJQ1989-10-30 View
510(k) K882539 CLEANTECH SYSTEMJKA1988-08-08 View
510(k) K874482 REVISED IMMUDIA HEM-SPKHE1988-05-13 View
510(k) K873986 BETA-HCG ASSAYDHA1988-02-02 View
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