FDA 510(k) Applications Submitted by CHUCK LINDLEY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000209 | 01/24/2000 | DOSE 1 | SCANDITRONIX WELLHOFER NORTH AMERICA |
| K092018 | 07/06/2009 | OMNIPRO INCLINE | IBA DOSIMETRY GMBH |
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