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FDA 510(k)

MSA100BT Peak Flow Meter

K-Number: K170281 · 2017-10-06

ApplicantBeijing M&B Electronic Instruments Co., Ltd.
Decision Date2017-10-06
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MSA100BT Peak Flow Meter is the device name listed in this FDA 510(k) record. The listed applicant is Beijing M&B Electronic Instruments Co., Ltd.. It received FDA 510(k) clearance on 2017-10-06 under 510(k) number K170281. 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 MSA100BT Peak Flow Meter?

MSA100BT Peak Flow Meter is a medical device that received FDA 510(k) clearance on 2017-10-06. The listed applicant is Beijing M&B Electronic Instruments Co., Ltd.. The 510(k) number is K170281.

When did MSA100BT Peak Flow Meter receive FDA 510(k) clearance?

MSA100BT Peak Flow Meter received FDA 510(k) clearance on 2017-10-06, under 510(k) number K170281.

Who is the listed applicant for MSA100BT Peak Flow Meter?

The FDA 510(k) record lists Beijing M&B Electronic Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MSA100BT Peak Flow Meter?

The FDA product code for MSA100BT 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.

K253180Microlife Digital Peak Flow Meter, Model PF200B (PF200B)Microlife CorporationK252802Peak Flow Meter (PF-10(BR-PEF231))Shenzhen Bi-Rich Medical Devices Co., Ltd.K241338Peak Flow MeterChongqing Moffy Innovation Technology Co., Ltd.K232588Aluna 2Knox Medical DiagnosticsK230423Electronic Peak Flow MeterTaian Dalu Medical Instrument Co., Ltd.K222810TD-7301 Peak Flow meterGostar Co., Ltd.

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.

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