FDA 510(k) Applications Submitted by DEBORA STAPLETON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K112511 | 08/30/2011 | DOBBHOFF DUAL PORT FEEDING TUBE | COVIDIEN LP, FORMERLY REGISTERED AS KENDALL |
| K073122 | 11/06/2007 | MONOJECT HYPODERMIC NEEDLE, MODEL 250, 30 GAUGE HYPODERMIC NEEDLE | COVIDIEN LP, FORMERLY REGISTERED AS TYCO HEALTHCAR |
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