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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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