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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 the device name listed in this FDA 510(k) record. The listed applicant is Taian Dalu Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2024-02-23 under 510(k) 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. The listed applicant is Taian Dalu Medical Instrument Co., Ltd.. The 510(k) number is K230423.

When did Electronic Peak Flow Meter receive FDA 510(k) clearance?

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

Who is the listed applicant for Electronic Peak Flow Meter?

The FDA 510(k) record lists Taian Dalu Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: BZH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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