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FDA 510(k)

Peak Flow Meter

K-Number: K241338 · 2024-12-31

Decision Date2024-12-31
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Peak Flow Meter is the device name listed in this FDA 510(k) record. The listed applicant is Chongqing Moffy Innovation Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-12-31 under 510(k) number K241338. 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 Peak Flow Meter?

Peak Flow Meter is a medical device that received FDA 510(k) clearance on 2024-12-31. The listed applicant is Chongqing Moffy Innovation Technology Co., Ltd.. The 510(k) number is K241338.

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

Peak Flow Meter received FDA 510(k) clearance on 2024-12-31, under 510(k) number K241338.

Who is the listed applicant for Peak Flow Meter?

The FDA 510(k) record lists Chongqing Moffy Innovation Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Peak Flow Meter?

The FDA product code for Peak Flow Meter is BZH.

Other records listing Chongqing Moffy Innovation Technology Co., Ltd. as applicant

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.

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