AIRCO 2000 SERIES FLOWMETERS
K-Number: K862797 · 1986-08-08
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Device Summary
Frequently Asked Questions
What is the AIRCO 2000 SERIES FLOWMETERS?
AIRCO 2000 SERIES FLOWMETERS is a medical device that received FDA 510(k) clearance on 1986-08-08. The listed applicant is Airco, Inc.. The 510(k) number is K862797.
When did AIRCO 2000 SERIES FLOWMETERS receive FDA 510(k) clearance?
AIRCO 2000 SERIES FLOWMETERS received FDA 510(k) clearance on 1986-08-08, under 510(k) number K862797.
Who is the listed applicant for AIRCO 2000 SERIES FLOWMETERS?
The FDA 510(k) record lists Airco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIRCO 2000 SERIES FLOWMETERS?
The FDA product code for AIRCO 2000 SERIES FLOWMETERS 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.
Other records listing Airco, 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: 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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