AIRWAY, ARGYLE NASOPHARYNGEAL
K-Number: K760125 · 1976-07-19
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Device Summary
Frequently Asked Questions
What is the AIRWAY, ARGYLE NASOPHARYNGEAL?
AIRWAY, ARGYLE NASOPHARYNGEAL is a medical device that received FDA 510(k) clearance on 1976-07-19. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760125.
When did AIRWAY, ARGYLE NASOPHARYNGEAL receive FDA 510(k) clearance?
AIRWAY, ARGYLE NASOPHARYNGEAL received FDA 510(k) clearance on 1976-07-19, under 510(k) number K760125.
Who is the listed applicant for AIRWAY, ARGYLE NASOPHARYNGEAL?
The FDA 510(k) record lists Sherwood Medical Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIRWAY, ARGYLE NASOPHARYNGEAL?
The FDA product code for AIRWAY, ARGYLE NASOPHARYNGEAL 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 Sherwood Medical Industries 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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