Medical Device Manufacturer · PH , Binan, Laguna

Terumo (Philippines) Corporation - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2012

Recent clearances: Terumo SurGuard 3 Safety Hypodermic Needle, TERUMO SURFLO I.V. CATHETER, TERUMO(R) NEEDLE

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.

510(k) submissions have been managed by Terumo Medical Corporation as regulatory consultant.

FDA 510(k) Regulatory Record - Terumo (Philippines) Corporation

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