Sil-Med Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
29
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K972521NAVIGATOR (STYLET) 2006October 1, 1997
K961392ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT IIJuly 18, 1997
K961194ANTIMICROBIAL MEDIASTINAL SILICONE DRAINAugust 8, 1996
K961295SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCARJune 26, 1996
K960099PENROSE DRAIN MODELS 6001 - 6007March 11, 1996
K955463GRIP-A-BOOTSJanuary 23, 1996
K942709MEDIASTINAL SILICONE DRAINSJanuary 4, 1996
K926496SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAINMay 24, 1995
K926408SIL-SLIP FLAT SUCTION DRAINFebruary 2, 1994
K926495SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPEFebruary 2, 1994
K921424SIL-MED FLAT SUCTION DRAINSeptember 28, 1992
K903989SIL-MED T-TUBE DRAINJanuary 31, 1991
K891471SIL-MED WASTE FLUID DUMP BAGAugust 15, 1989
K885167TRUDELL BENT CATHETERJanuary 31, 1989
K862767SILICONE SUMP DRAINAugust 7, 1986
K854418ROUND SUCTION DRAINNovember 19, 1985
K851195VASCULAR ACCESS CATHETERJune 7, 1985
K851196INCISION DRAINJune 4, 1985
K851921Y CONNECTORMay 17, 1985
K850247PERITONEAL DIALYSIS COIL CATHETERFebruary 14, 1985