FDA 510(k) Applications Submitted by EAGLE VISION, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030353 | 02/03/2003 | MONOCANALICULAR STENTS, LACRIMAL INTUBATION SETS | EAGLE VISION, INC. |
| K053333 | 12/01/2005 | EAGLEVISION GELLANSERTS, MODEL REF 0040 | EAGLE VISION, INC. |
| K991130 | 04/02/1999 | FLEXPLUG | EAGLE VISION, INC. |
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