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Schiff & Co.

15 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
X-TIP INTRAOSSEOUS PERFORATOR (K990511)Schiff & Co.1999-04-27
JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 (K982136)Schiff & Co.1999-03-24
NUTRISAFE ENTERAL FEEDING TUBE (K981629)Schiff & Co.1999-02-04
VYGON DOUBLE LUMEN UMBILICAL CATHETER (K981630)Schiff & Co.1998-10-01
PLUS REUSABLE RESUSCITATOR (K974141)Schiff & Co.1998-05-21
VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM (K954448)Schiff & Co.1996-10-28
HM-CAP EIA TEST (MODIFICATION) (K955085)Schiff & Co.1996-02-09
HM-CAP EIA KIT (K944159)Schiff & Co.1995-07-18
VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE (K943521)Schiff & Co.1995-02-14
KEMBLE LIQUID HANDLING SYSTEM DISPENSER (K896684)Schiff & Co.1990-04-16
OLYMPUS PK-TP SYSTEM REACTIVE CONTROL (K894617)Schiff & Co.1989-10-31
FASTEC 901 AGGLUTINATION PATTERN READER (K895967)Schiff & Co.1989-10-30
CLEANTECH SYSTEM (K882539)Schiff & Co.1988-08-08
REVISED IMMUDIA HEM-SP (K874482)Schiff & Co.1988-05-13
BETA-HCG ASSAY (K873986)Schiff & Co.1988-02-02

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