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FDA 510(k) Applications Submitted by CAROL C RYERSON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K021829
06/04/2002
MODIFICATION TO KODAK DIRECTVIEW CR 800/900 SYSTEM
EASTMAN KODAK COMPANY
K102242
08/09/2010
OSOM C. DIFFICILE TOXIN A/B TEST
GENZYME CORPORATION
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