Tyco Healthcare

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K071049DOVER 100% SILICONE FOLEY CATHETER WITH TEMPERATURE SENSOROctober 16, 2007
K070685KENDALL ANTIMICROBIAL DRAIN DRESSING FOR OTC USE, MODEL 6662September 14, 2007
K070653KENDALL KERLIX ANTIMICROBIAL SUPER SPONGE DRESSING FOR OTC USE, MODEL 6662September 12, 2007
K061492MONOJECT MAGELLAN INSULIN AND TUBERCULIN SAFETY SYRINGEAugust 3, 2006
K042709DOVER SILVER TEMPERATURE SENSING FOLEY CATHETERJanuary 18, 2005
K040897DOVER ROB-NEL CATHETERJuly 20, 2004
K040649KENDALL SCD EXPRESS KAMBIA THIGH LENGTH TEARAWAY SLEEVEJuly 15, 2004
K041243DOVER RED RUBBER ROBINSON CATHETERJuly 7, 2004
K032438MODIFICATION TO: MONOJET PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE, MONOJET PREFILL HEPRIN LOCK FLUJune 30, 2004
K033453KENDALL ULTEC PRO AG+ HYDROCOLLOID DRESSINGApril 29, 2004
K032827KENDALL LIFETRACE UMBILICAL BLOOD COLLECTION KIT, CODE 56501December 8, 2003
K033373MONOJECT INSULIN SYRINGENovember 13, 2003
K013556MONOJECT PREFILL HEPARIN LOCK FLUSH SYRINGEDecember 31, 2001
K012736MONOJECT SAFETY NEEDLEOctober 25, 2001