Bistos Co., Ltd.
Bistos Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2025.
Top product codes for Bistos Co., Ltd.
Recent clearances by Bistos Co., Ltd.
- K251512 — Hi bebe super (BT-150B)
- K232991 — BT-1000
- K210289 — Infant Phototherapy Equipment
- K200675 — Hi bebe super (Models BT-150S and BT-150L)
- K160274 — Hi bebe plus
- K142799 — Model BT-220L and BT-220C
- K132543 — INFANT INCUBATOR
- K121267 — BT-200V VASCULAR DOPPLER
- K103545 — BT-350
- K100885 — FETAL MONITOR MODEL: BT-200T
- K052190 — FETAL MONITOR, MODELS BT-300 AND BT-200
Data sourced from openFDA. This site is unofficial and independent of the FDA.