MODIFICATION TO TRUZONE PEAK FLOW METER
K-Number: K991212 · 1999-07-01
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO TRUZONE PEAK FLOW METER?
MODIFICATION TO TRUZONE PEAK FLOW METER is a medical device that received FDA 510(k) clearance on 1999-07-01. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K991212.
When did MODIFICATION TO TRUZONE PEAK FLOW METER receive FDA 510(k) clearance?
MODIFICATION TO TRUZONE PEAK FLOW METER received FDA 510(k) clearance on 1999-07-01, under 510(k) number K991212.
Who is the listed applicant for MODIFICATION TO TRUZONE PEAK FLOW METER?
The FDA 510(k) record lists Monaghan Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO TRUZONE PEAK FLOW METER?
The FDA product code for MODIFICATION TO TRUZONE 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 Monaghan Medical 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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