Terumo (Philippines) Corporation - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Terumo (Philippines) Corporation has 5 FDA 510(k) cleared medical devices. Based in Binan, Laguna, PH.
Historical record: 5 cleared submissions from 2012 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Terumo (Philippines) Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Terumo (Philippines) Corporation
5 devices
Cleared
Oct 16, 2015
Terumo SurGuard 3 Safety Hypodermic Needle
General Hospital
57d
Cleared
Jun 12, 2014
TERUMO SURFLO I.V. CATHETER
General Hospital
230d
Cleared
Nov 08, 2012
TERUMO(R) NEEDLE
General Hospital
160d
Cleared
Aug 28, 2012
TERUMO SURGUARD3 SAFETY NEEDLE & HYPODERMIC SYRINGE WITH SAFETY NEEDLE
General Hospital
32d
Cleared
Mar 05, 2012
TERUMO SURGUARD 3 SAFETY NEEDLE TERUMO SURGUARD 3 HYPODERMIC SYRINGE WITH...
General Hospital
105d