Single-use Flexible Rhinolaryngoscope; Digital Video Monitor
K-Number: K230536 · 2023-06-14
Device Summary
Frequently Asked Questions
What is the Single-use Flexible Rhinolaryngoscope; Digital Video Monitor?
Single-use Flexible Rhinolaryngoscope; Digital Video Monitor is a medical device that received FDA 510(k) clearance on 2023-06-14. It is manufactured by Hunan Vathin Medical Instrument Co., Ltd.. The 510(k) number is K230536.
When was Single-use Flexible Rhinolaryngoscope; Digital Video Monitor approved by the FDA?
Single-use Flexible Rhinolaryngoscope; Digital Video Monitor received FDA 510(k) clearance on 2023-06-14, under approval number K230536.
What company makes Single-use Flexible Rhinolaryngoscope; Digital Video Monitor?
Single-use Flexible Rhinolaryngoscope; Digital Video Monitor is manufactured by Hunan Vathin Medical Instrument Co., Ltd..
What is the FDA product code for Single-use Flexible Rhinolaryngoscope; Digital Video Monitor?
The FDA product code for Single-use Flexible Rhinolaryngoscope; Digital Video Monitor is EOB.
Related Clinical Trials
Other Devices by Hunan Vathin Medical Instrument Co., Ltd.
Related Devices (Code: EOB)
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.