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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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