FDA 510(k) Applications Submitted by GYNETECH PTY. LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150519 | 03/02/2015 | ManipulatOR PRO, ManipulatOR | GYNETECH PTY. LTD. |
| K051594 | 06/16/2005 | MCCARTNEY ACCESS TUBE | GYNETECH PTY. LTD. |
| K142164 | 08/06/2014 | MANIPULATOR; MANIPULATOR PRO | GYNETECH PTY. LTD. |
| K142700 | 09/22/2014 | InsufflatOR Needle | GYNETECH PTY. LTD. |
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