FDA 510(k) Applications Submitted by NEOVISION CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K980423 | 02/03/1998 | SONOPSY LA SYSTEM | NEOVISION CORP. |
| K951999 | 04/28/1995 | HOLOPSY SYSTEM | NEOVISION CORP. |
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