FDA 510(k) Applications Submitted by SIGHTLINE TECHNOLOGIES LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K994130 | 12/07/1999 | RECTOSIGHT RS 300-04 | SIGHTLINE TECHNOLOGIES LTD. |
| K032688 | 08/29/2003 | COLONOSIGHT MODEL 510B | SIGHTLINE TECHNOLOGIES LTD. |
| K011825 | 06/11/2001 | RECTOSIGHT RS300-04;AND PROTOSIGHT PS300-04 DEVICE | SIGHTLINE TECHNOLOGIES LTD. |
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