MONITOR, AIRWAY PRESSURE
K-Number: K802955 · 1980-12-19
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Device Summary
Frequently Asked Questions
What is the MONITOR, AIRWAY PRESSURE?
MONITOR, AIRWAY PRESSURE is a medical device that received FDA 510(k) clearance on 1980-12-19. The listed applicant is Novametrix Medical Systems, Inc.. The 510(k) number is K802955.
When did MONITOR, AIRWAY PRESSURE receive FDA 510(k) clearance?
MONITOR, AIRWAY PRESSURE received FDA 510(k) clearance on 1980-12-19, under 510(k) number K802955.
Who is the listed applicant for MONITOR, AIRWAY PRESSURE?
The FDA 510(k) record lists Novametrix Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MONITOR, AIRWAY PRESSURE?
The FDA product code for MONITOR, AIRWAY PRESSURE 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 Novametrix Medical Systems, 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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