Medical Device Manufacturer · GB , England Ct21 6db

Portex , Ltd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2003

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Portex , Ltd. Obstetrics & Gynecology ✕

2 devices

1-2 of 2

Cleared Dec 19, 2003

WALLACE (SURE VIEW) EMBRYO REPLACEMENT CATHETER AND TRIAL TRANSFER CATHETER

Obstetrics & Gynecology · 81d

Cleared Jun 26, 2003

WALLACE DUAL LUMEN OOCYTE RETRIEVAL SETS

Obstetrics & Gynecology · 34d