Mutoh America Co., Ltd.

Mutoh America Co., Ltd. holds 1 FDA 510(k) medical device clearance, cleared in 2001.

Top product codes for Mutoh America Co., Ltd.

LFL — Unknown1 device

Recent clearances by Mutoh America Co., Ltd.

K010309 — SONOPET MODEL UST-2001 ULTRASONIC SURGICAL ASPIRATORCode LFL·2001-04-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.