Terumo Corp.
Terumo Corp. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2010.
Top product codes for Terumo Corp.
Recent clearances by Terumo Corp.
- K100282 — TERUMO SURSHIELD- PUR SAFETY I.V. CATHETER
- K092372 — HEARTRAIL III GUIDING CATHETER
- K091417 — SINGLE USE GUIDEWIRE, MODELS G-240-2527S, G-240-2545S, G-240-2527A, G-240-2545A, G-240-3527S, G-240-3545S & G-240-3527A
- K090973 — TERUMO SURSHIELD SAFETY I.V. CATHETER (18G X 51MM & 20G X 51MM SIZES)
- K073474 — CAPIOX CIRCUIT CONNECTORS
- K071572 — CAPIOX FX05 HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER
- K071494 — CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR AND ARTERIAL FILTER
- K071075 — TERUMO DIGITAL BLOOD PRESSURE MONITOR ES-H55A
- K040783 — FOUNDATION
- K040210 — CAPIOX RX25 HOLLOW FIBER OXYGENATOR W/WO HARDSHELL RESERVOIR
- K033681 — GLIDESHEATH
- K031266 — SURSHIELD SAFETY WINGED INFUSION SET
- K030449 — MODIFICATION TO CAPIOX SX10 HARDSHELL RESERVOIR
- K022115 — CAPIOX RX05 HOLLOW FIBER OXYGENATOR W/WITHOUT HARDSHELL RESERVOIR
- K003371 — PUMP TUBING WITH X-COATING
- K993189 — CARDIOPULMONARY BYPASS PUMP TUBING - 1/4 INCH TUBING, CARDIOPULMONARY BYPASS PUMP TUBING - 3/8 INCH TUBING
- K983490 — TERUMO VENOJECT,LUER ADAPTER
- K980796 — TERUMO ALLERGY SYRINGE
- K943861 — CAPIOX SP PUMP HEAD
- K910969 — TORQUE DEVICE FOR A GUIDE WIRE
- K910722 — 450CM GUIDE WIRE FOR G.I. USE
Data sourced from openFDA. This site is unofficial and independent of the FDA.