WRIGHT POCKET PEAK FLOW METER
K-Number: K924343 · 1993-06-16
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Device Summary
Frequently Asked Questions
What is the WRIGHT POCKET PEAK FLOW METER?
WRIGHT POCKET PEAK FLOW METER is a medical device that received FDA 510(k) clearance on 1993-06-16. The listed applicant is Ferraris Medical, Inc.. The 510(k) number is K924343.
When did WRIGHT POCKET PEAK FLOW METER receive FDA 510(k) clearance?
WRIGHT POCKET PEAK FLOW METER received FDA 510(k) clearance on 1993-06-16, under 510(k) number K924343.
Who is the listed applicant for WRIGHT POCKET PEAK FLOW METER?
The FDA 510(k) record lists Ferraris Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WRIGHT POCKET PEAK FLOW METER?
The FDA product code for WRIGHT POCKET PEAK FLOW METER 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 Ferraris Medical, 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.
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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