RESPIRGARD
K-Number: K802763 · 1980-11-26
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Device Summary
Frequently Asked Questions
What is the RESPIRGARD?
RESPIRGARD is a medical device that received FDA 510(k) clearance on 1980-11-26. The listed applicant is Marquest Medical Products, Inc.. The 510(k) number is K802763.
When did RESPIRGARD receive FDA 510(k) clearance?
RESPIRGARD received FDA 510(k) clearance on 1980-11-26, under 510(k) number K802763.
Who is the listed applicant for RESPIRGARD?
The FDA 510(k) record lists Marquest Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RESPIRGARD?
The FDA product code for RESPIRGARD is CAH.
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 Marquest Medical 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: CAH)
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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