AIRWAY PRESSURE MONITOR
K-Number: K840420 · 1984-04-05
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Device Summary
Frequently Asked Questions
What is the AIRWAY PRESSURE MONITOR?
AIRWAY PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K840420.
When did AIRWAY PRESSURE MONITOR receive FDA 510(k) clearance?
AIRWAY PRESSURE MONITOR received FDA 510(k) clearance on 1984-04-05, under 510(k) number K840420.
Who is the listed applicant for AIRWAY PRESSURE MONITOR?
The FDA 510(k) record lists Respiratory Support Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIRWAY PRESSURE MONITOR?
The FDA product code for AIRWAY PRESSURE MONITOR is CAP.
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 Respiratory Support Products, 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: CAP)
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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