FDA 510(k) Applications Submitted by MICHAEL P DAYTON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K140138 | 01/22/2014 | HEARTNAVIGATOR RELEASE 2.0 | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| K990227 | 01/25/1999 | ULTRASHAPER KERATOME | LASERSIGHT TECHNOLOGIES, INC. |
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