FDA 510(k) Applications Submitted by MARK MASON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K022630 | 08/07/2002 | MODIFICATION TO FOCUS | INSTRUMENTARIUM CORP. |
| K043612 | 12/30/2004 | ORTHOPANTOMOGRAPH OP200, OP200D, AND ORTHOCEPH OC200, OC200D | INSTRUMENTARIUM CORP. IMAGING DIVISION |
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