Tyco Healthcare
FDA 510(k) & PMA Approved Devices — 14 products
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Total Devices14
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K071049 | DOVER 100% SILICONE FOLEY CATHETER WITH TEMPERATURE SENSOR | EZL | 2007-10-16 | View |
| 510(k) | K070685 | KENDALL ANTIMICROBIAL DRAIN DRESSING FOR OTC USE, MODEL 6662 | FRO | 2007-09-14 | View |
| 510(k) | K070653 | KENDALL KERLIX ANTIMICROBIAL SUPER SPONGE DRESSING FOR OTC USE, MODEL 6662 | FRO | 2007-09-12 | View |
| 510(k) | K061492 | MONOJECT MAGELLAN INSULIN AND TUBERCULIN SAFETY SYRINGE | FMF | 2006-08-03 | View |
| 510(k) | K042709 | DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER | EZL | 2005-01-18 | View |
| 510(k) | K040897 | DOVER ROB-NEL CATHETER | KOD | 2004-07-20 | View |
| 510(k) | K040649 | KENDALL SCD EXPRESS KAMBIA THIGH LENGTH TEARAWAY SLEEVE | JOW | 2004-07-15 | View |
| 510(k) | K041243 | DOVER RED RUBBER ROBINSON CATHETER | KOD | 2004-07-07 | View |
| 510(k) | K032438 | MODIFICATION TO: MONOJET PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE, MONOJET PREFILL HEPRIN LOCK FLUSH SYRINGE | NGT | 2004-06-30 | View |
| 510(k) | K033453 | KENDALL ULTEC PRO AG+ HYDROCOLLOID DRESSING | FRO | 2004-04-29 | View |
| 510(k) | K032827 | KENDALL LIFETRACE UMBILICAL BLOOD COLLECTION KIT, CODE 56501 | KSR | 2003-12-08 | View |
| 510(k) | K033373 | MONOJECT INSULIN SYRINGE | FMI | 2003-11-13 | View |
| 510(k) | K013556 | MONOJECT PREFILL HEPARIN LOCK FLUSH SYRINGE | FOZ | 2001-12-31 | View |
| 510(k) | K012736 | MONOJECT SAFETY NEEDLE | FMI | 2001-10-25 | View |
No matching devices.
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