Flexible Cystoscope (Model: CY50H-20EU, CY50H-20US, CY55H-24EU, CY55H-24US)
K-Number: K222162 · 2022-11-09
Device Summary
Frequently Asked Questions
What is the Flexible Cystoscope (Model: CY50H-20EU, CY50H-20US, CY55H-24EU, CY55H-24US)?
Flexible Cystoscope (Model: CY50H-20EU, CY50H-20US, CY55H-24EU, CY55H-24US) is a medical device that received FDA 510(k) clearance on 2022-11-09. It is manufactured by Shanghai AnQing Medical Instrument Co., Ltd.. The 510(k) number is K222162.
When was Flexible Cystoscope (Model: CY50H-20EU, CY50H-20US, CY55H-24EU, CY55H-24US) approved by the FDA?
Flexible Cystoscope (Model: CY50H-20EU, CY50H-20US, CY55H-24EU, CY55H-24US) received FDA 510(k) clearance on 2022-11-09, under approval number K222162.
What company makes Flexible Cystoscope (Model: CY50H-20EU, CY50H-20US, CY55H-24EU, CY55H-24US)?
Flexible Cystoscope (Model: CY50H-20EU, CY50H-20US, CY55H-24EU, CY55H-24US) is manufactured by Shanghai AnQing Medical Instrument Co., Ltd..
What is the FDA product code for Flexible Cystoscope (Model: CY50H-20EU, CY50H-20US, CY55H-24EU, CY55H-24US)?
The FDA product code for Flexible Cystoscope (Model: CY50H-20EU, CY50H-20US, CY55H-24EU, CY55H-24US) is FAJ.
Other Devices by Shanghai AnQing Medical Instrument Co., Ltd.
Related Devices (Code: FAJ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.