Goodman Co., Ltd.
Goodman Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2025.
Top product codes for Goodman Co., Ltd.
Recent clearances by Goodman Co., Ltd.
- K243944 — Aperta NSE PTA Balloon Dilatation Catheter
- K232013 — Aperta NSE PTA Balloon Dilatation Catheter (AW18-05040040/AA18-05040040, AW18-09040040/AA18-09040040, AW18-14540040, AW18-05050040/AA18-05050040, AW18-09050040/AA18-09050040, AW18-14550040, AW18-05060040/AA18-05060040, AW18-09060040/AA18-09060040, AW18-14560040 AW18-05070040/AA18-05070040, AW18-09070040/AA18-09070040, AW18-14570040, AW18-05080040/AA18-05080040, AW18-09080040/AA18-09080040, AW18-14580040)
- K010763 — GOODNET
Data sourced from openFDA. This site is unofficial and independent of the FDA.