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FDA 510(k)

Single-use Flexible Rhinolaryngoscope; Digital Video Monitor

K-Number: K230536 · 2023-06-14

Decision Date2023-06-14
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Single-use Flexible Rhinolaryngoscope; Digital Video Monitor is a medical device manufactured by Hunan Vathin Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2023-06-14 under approval number K230536. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

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

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Official Source

View on FDA Database →

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