NASOPHARYNGEAL AIRWAY
K-Number: K810960 · 1981-04-23
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Device Summary
Frequently Asked Questions
What is the NASOPHARYNGEAL AIRWAY?
NASOPHARYNGEAL AIRWAY is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Vesta, Inc.. The 510(k) number is K810960.
When did NASOPHARYNGEAL AIRWAY receive FDA 510(k) clearance?
NASOPHARYNGEAL AIRWAY received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810960.
Who is the listed applicant for NASOPHARYNGEAL AIRWAY?
The FDA 510(k) record lists Vesta, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NASOPHARYNGEAL AIRWAY?
The FDA product code for NASOPHARYNGEAL AIRWAY is BTQ.
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 Vesta, 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: BTQ)
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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