MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100
K-Number: K031024 · 2003-11-14
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Device Summary
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.
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
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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