Microlife Digital Peak Flow Meter, Model PF200B (PF200B)
K-Number: K253180 · 2026-06-23
Device Summary
Frequently Asked Questions
What is the Microlife Digital Peak Flow Meter, Model PF200B (PF200B)?
Microlife Digital Peak Flow Meter, Model PF200B (PF200B) is a medical device that received FDA 510(k) clearance on 2026-06-23. The listed applicant is Microlife Corporation. The 510(k) number is K253180.
When did Microlife Digital Peak Flow Meter, Model PF200B (PF200B) receive FDA 510(k) clearance?
Microlife Digital Peak Flow Meter, Model PF200B (PF200B) received FDA 510(k) clearance on 2026-06-23, under 510(k) number K253180.
Who is the listed applicant for Microlife Digital Peak Flow Meter, Model PF200B (PF200B)?
The FDA 510(k) record lists Microlife Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Microlife Digital Peak Flow Meter, Model PF200B (PF200B)?
The FDA product code for Microlife Digital Peak Flow Meter, Model PF200B (PF200B) is BZH.
Other records listing Microlife Corporation 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.