FDA 510(k)

THE PEAK

K-Number: K920390 · 1992-09-11

Decision Date1992-09-11

Product CodeBZH

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

THE PEAK is the device name listed in this FDA 510(k) record. The listed applicant is Multispiro, Inc.. It received FDA 510(k) clearance on 1992-09-11 under 510(k) number K920390. 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 THE PEAK?

THE PEAK is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Multispiro, Inc.. The 510(k) number is K920390.

When did THE PEAK receive FDA 510(k) clearance?

THE PEAK received FDA 510(k) clearance on 1992-09-11, under 510(k) number K920390.

Who is the listed applicant for THE PEAK?

The FDA 510(k) record lists Multispiro, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE PEAK?

The FDA product code for THE PEAK is BZH.

Other records listing Multispiro, Inc. 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.

K915451MULTISPIRO-SX K913681MULTISPIRO-BREEZE

Related Devices (Code: BZH)

K253180Microlife Digital Peak Flow Meter, Model PF200B (PF200B)Microlife Corporation K252802Peak Flow Meter (PF-10(BR-PEF231))Shenzhen Bi-Rich Medical Devices Co., Ltd.K241338Peak Flow MeterChongqing Moffy Innovation Technology Co., Ltd.K232588Aluna 2Knox Medical Diagnostics K230423Electronic Peak Flow MeterTaian Dalu Medical Instrument Co., Ltd.K222810TD-7301 Peak Flow meterGostar Co., Ltd.

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.