FDA 510(k) Applications Submitted by CAROL 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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