The Kendal Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
63
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K000087MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FRMarch 17, 2000
K990500KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL September 28, 1999
K991758MONOJECT INSULIN SYRINGEJune 14, 1999
K970969KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SETApril 23, 1997
K951488KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAPApril 25, 1995
K942664KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEMJanuary 17, 1995
K942774POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSINGJuly 20, 1994
K892434KENDALL CURITY OXYGEN MASKAugust 15, 1989
K892438KENDALL CURITY INTRAVASCULAR CUT DOWN TUBESJuly 24, 1989
K892440KENDALL CURITY EXTENSION TUBESJuly 24, 1989
K892436KENDALL CURITY IRRIGATION SYRINGEJuly 14, 1989
K892442KENDALL CURITY URETHRAL CATHETERSJune 23, 1989
K892439KENDALL CURITY STOMACH TUBESJune 23, 1989
K892437KENDALL KENGUARD URINARY LEG BAGSJune 23, 1989
K892435KENDALL CURITY OXYGEN NASAL CANNULAJune 12, 1989
K892432KENDALL CURITY ENDOTRACHEAL TUBESJune 12, 1989
K892441KENDALL CURITY SUCTION CATHETERSMay 31, 1989
K892431KENDALL CURITY FEEDING TUBESMay 19, 1989
K892433KENDALL CURITY URINARY DRAINAGE BAGSMay 5, 1989
K885238CURITY CONTINUOUS SPINAL ANESTHESIA TRAYFebruary 22, 1989