RESPIRATORY THERAPY FLOWMETER
K-Number: K802659 · 1980-11-12
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Device Summary
Frequently Asked Questions
What is the RESPIRATORY THERAPY FLOWMETER?
RESPIRATORY THERAPY FLOWMETER is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Design & Manufacturing Consultants. The 510(k) number is K802659.
When did RESPIRATORY THERAPY FLOWMETER receive FDA 510(k) clearance?
RESPIRATORY THERAPY FLOWMETER received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802659.
Who is the listed applicant for RESPIRATORY THERAPY FLOWMETER?
The FDA 510(k) record lists Design & Manufacturing Consultants as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RESPIRATORY THERAPY FLOWMETER?
The FDA product code for RESPIRATORY THERAPY FLOWMETER is CAX.
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.
Related Devices (Code: CAX)
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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