Alpinion Medical Systems Co., Ltd.
Alpinion Medical Systems Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2023.
Top product codes for Alpinion Medical Systems Co., Ltd.
Recent clearances by Alpinion Medical Systems Co., Ltd.
- K223564 — X-CUBE 50, X-CUBE 60
- K221093 — X-CUBE 70, X-CUBE 90
- K220857 — X-CUBE 50, X-CUBE 60
- K213523 — X-CUBE i8, X-CUBE i9
- K211299 — X-CUBE 70
- K211300 — X-CUBE 90
- K200449 — X-Cube 90
- K200450 — X-Cube 70
- K182594 — E-CUBE i7
- K182845 — minisono
- K181617 — E-CUBE 8
- K181277 — E-CUBE 12
- K172732 — E-CUBE 8
- K161439 — E-CUBE 11
- K153424 — E-CUBE i7
- K150773 — E-CUBE 15 Diagnostic Ultrasound System
- K142733 — E-CUBE 5
- K142884 — E-CUBE 12
- K132687 — E-CUBE 7
- K123610 — E-CUBE 15
- K123611 — E-CUBE 7
- K121729 — E-CUBE 7
- K121888 — E-CUBE 15
- K121937 — E-CUBE INNO
- K120060 — E-CUBE 9
- K111864 — E-CUBE 9
Data sourced from openFDA. This site is unofficial and independent of the FDA.