Medical Device Manufacturer · US , Keene , NH

Concord/Portex - FDA 510(k) Cleared Devices

23 submissions · 20 cleared · Since 1989

23

Total

20

Cleared

0

Denied

FDA 510(k) Regulatory Record - Concord/Portex General Hospital ✕

4 devices

1-4 of 4

Cleared Jul 27, 1993

SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES

General Hospital · 193d

Cleared Apr 29, 1993

NEEDLE-PRO CARTRIDGE

General Hospital · 307d

Cleared May 03, 1991

SAFETY NEEDLE SHEATH, MODIFICATION

General Hospital · 63d

Cleared Dec 19, 1990

SAFETY NEEDLE SHEATH

General Hospital · 98d