FDA 510(k) Applications Submitted by SANKO X-RAY MANUFACTURING CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K972921 | 08/08/1997 | SANKO INTRAORAL DENTAL X-RAY | SANKO X-RAY MANUFACTURING CO., LTD. |
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