FDA 510(k) Applications Submitted by T.WHIT ATHEY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990202 | 01/21/1999 | SUGITA TITANIUM ANEURYSM CLIP | MIZUHO AMERICA, INC. |
| K012010 | 06/27/2001 | MODIFICATION TO LR 5200 FILM RECORDER | AGFA CORP. |
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