FDA 510(k) Applications Submitted by TOMEY CORPORATION USA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971953 | 05/28/1997 | CONFOSCAN | TOMEY CORPORATION USA |
| K971685 | 05/07/1997 | IMAGESCAPE DIGITAL RETINAL IMAGE SYSTEM | TOMEY CORPORATION USA |
| K961805 | 05/10/1996 | TOMEY DTL ELECTRODE | TOMEY CORPORATION USA |
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