Medical Device Manufacturer · US , Walker , MI

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

20 submissions · 20 cleared · Since 1977

20

Total

20

Cleared

0

Denied

FDA 510(k) Regulatory Record - Portex, Inc. General Hospital ✕

2 devices

1-2 of 2

Cleared Feb 13, 2002

HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE

General Hospital · 65d

Cleared Mar 14, 1977

SPECIMEN COLLECTOR

General Hospital · 54d