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FDA 510(k)

Electronic Peak Flow Meter

K-Number: K230423 · 2024-02-23

Decision Date2024-02-23
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Electronic Peak Flow Meter is a medical device manufactured by Taian Dalu Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2024-02-23 under approval number K230423. The device is classified under product code BZH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Electronic Peak Flow Meter?

Electronic Peak Flow Meter is a medical device that received FDA 510(k) clearance on 2024-02-23. It is manufactured by Taian Dalu Medical Instrument Co., Ltd.. The 510(k) number is K230423.

When was Electronic Peak Flow Meter approved by the FDA?

Electronic Peak Flow Meter received FDA 510(k) clearance on 2024-02-23, under approval number K230423.

What company makes Electronic Peak Flow Meter?

Electronic Peak Flow Meter is manufactured by Taian Dalu Medical Instrument Co., Ltd..

What is the FDA product code for Electronic Peak Flow Meter?

The FDA product code for Electronic Peak Flow Meter is BZH.

Related Clinical Trials

Related Devices (Code: BZH)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.