FDA 510(k) Applications Submitted by OPHELIA BIGGS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190392 | 02/19/2019 | WaveLight FS200 Patient Interface | Alcon Laboratories, Inc. |
| K111697 | 06/17/2011 | AMO WHITESTAR SIGNATURE PHACOEMULSIFICATION SYSTEM | ABBOTT MEDICAL OPTICS INC |
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