Schiff & Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K990511X-TIP INTRAOSSEOUS PERFORATORApril 27, 1999
K982136JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200March 24, 1999
K981629NUTRISAFE ENTERAL FEEDING TUBEFebruary 4, 1999
K981630VYGON DOUBLE LUMEN UMBILICAL CATHETEROctober 1, 1998
K974141PLUS REUSABLE RESUSCITATORMay 21, 1998
K954448VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEMOctober 28, 1996
K955085HM-CAP EIA TEST (MODIFICATION)February 9, 1996
K944159HM-CAP EIA KITJuly 18, 1995
K943521VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTUREFebruary 14, 1995
K896684KEMBLE LIQUID HANDLING SYSTEM DISPENSERApril 16, 1990
K894617OLYMPUS PK-TP SYSTEM REACTIVE CONTROLOctober 31, 1989
K895967FASTEC 901 AGGLUTINATION PATTERN READEROctober 30, 1989
K882539CLEANTECH SYSTEMAugust 8, 1988
K874482REVISED IMMUDIA HEM-SPMay 13, 1988
K873986BETA-HCG ASSAYFebruary 2, 1988