DOVER ROB-NEL CATHETER— 510(k) K040897
Substantially EquivalentTyco Healthcare
FDA 510(k) clearance K040897 for DOVER ROB-NEL CATHETER, Substantially Equivalent on 2004-07-20. Applicant: Tyco Healthcare. Device class: 2.
Clearance details
- Applicant
- Tyco Healthcare
- Product code
- Code KOD
- Device class
- Class 2
- Regulation
- 21 CFR 876.5130
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mansfield, MA, US
Recent devices under product code KOD
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view all- K071049 — DOVER 100% SILICONE FOLEY CATHETER WITH TEMPERATURE SENSOR
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- K070653 — KENDALL KERLIX ANTIMICROBIAL SUPER SPONGE DRESSING FOR OTC USE, MODEL 6662
- K061492 — MONOJECT MAGELLAN INSULIN AND TUBERCULIN SAFETY SYRINGE
- K042709 — DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER
Adverse events under product code KOD
product code KOD- Death
- 5
- Injury
- 1,129
- Malfunction
- 7,019
- Total
- 8,153
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.