FDA 510(k) Applications Submitted by SCHIFF & CO.

FDA 510(k) Number Submission Date Device Name Applicant
K981629 05/07/1998 NUTRISAFE ENTERAL FEEDING TUBE SCHIFF & CO.
K981630 05/07/1998 VYGON DOUBLE LUMEN UMBILICAL CATHETER SCHIFF & CO.
K982136 06/17/1998 JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 SCHIFF & CO.
K974141 11/03/1997 PLUS REUSABLE RESUSCITATOR SCHIFF & CO.
K954448 09/25/1995 VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM SCHIFF & CO.
K955085 10/26/1995 HM-CAP EIA TEST (MODIFICATION) SCHIFF & CO.
K990511 02/18/1999 X-TIP INTRAOSSEOUS PERFORATOR SCHIFF & CO.


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