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FDA 510(k)

MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100

K-Number: K031024 · 2003-11-14

Decision Date2003-11-14
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100 is the device name listed in this FDA 510(k) record. The listed applicant is Microlife Corp.. It received FDA 510(k) clearance on 2003-11-14 under 510(k) number K031024. 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 MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100?

MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100 is a medical device that received FDA 510(k) clearance on 2003-11-14. The listed applicant is Microlife Corp.. The 510(k) number is K031024.

When did MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100 receive FDA 510(k) clearance?

MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100 received FDA 510(k) clearance on 2003-11-14, under 510(k) number K031024.

Who is the listed applicant for MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100?

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

What is the FDA product code for MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100?

The FDA product code for MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100 is BZH.

Related Clinical Trials

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.

Other records listing Microlife Corp. 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.

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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.

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