Terumo America, Inc.
Terumo America, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1981.
Top product codes for Terumo America, Inc.
Recent clearances by Terumo America, Inc.
- K811523 — PLASMA FLEX
- K802970 — TERUMO HOLLOW FIBER OXYGENATOR
- K802122 — CLIRANS TH13 HOLLOW FIBER DIALYZER
- K802441 — CLIRANS TH10 HOLLOW FIBER DIALYZER
- K801192 — CLIRANS TE10 HOLLOW FIBER DIALYZER
- K801193 — CLIRANS TE15 HOLLOW FIBER DIALYZER
- K801194 — CLIRANS TE07 HOLLOW FIBER DIALYZER
- K791411 — COAXIAL DUAL FLOW CATHETER
- K791173 — SURFLO INJECTION PLUG
- K790105 — TERUMO IMUGARD
- K772362 — AVF SET FOR SINGLE NEEDLE HEMODIALYSIS
- K772040 — TRANSDUCER PROTECTOR
- K771431 — ARTIFICIAL K-NOSE BREATHAID
- K771432 — HICALIQ IVH BAG
- K771430 — BLOOD FILTER, W/SET
- K771693 — CLIRANS BLOOD LINES SET
- K771694 — CLIRANS TH 15 HOLLOW FIBER DIALYZER
- K771212 — SAFEED DISP. PLASTIC CATHETER
- K771458 — INFUSION ACCELERATOR
- K771454 — MICRO SYRINGE & NEEDLE
- K771209 — TERUFUSION BLOOD ADMIN. SET
- K771206 — AV FISTULA NEEDLE SET
- K771203 — DISP. HYPODERMIC NEEDLE
- K771204 — SURFLO WINGED INFUSION SET
- K771205 — HYPODERMIC SYRINGE
- K771207 — TERUFUSION DONOR SET
- K771211 — DOPPLER (UTD-5 & UTD-6)
- K771210 — UROGARD URINARY DRAINAGE BAG
- K770422 — CATHETER, SURFLO, I.V.
- K760948 — THERMO FINER CORETEMP
- K760775 — TERUMO DISPOSABLE SPINAL NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.