ARGYLE NASAL CANNULA
K-Number: K833127 · 1983-11-03
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Device Summary
Frequently Asked Questions
What is the ARGYLE NASAL CANNULA?
ARGYLE NASAL CANNULA is a medical device that received FDA 510(k) clearance on 1983-11-03. The listed applicant is Sherwood Medical Co.. The 510(k) number is K833127.
When did ARGYLE NASAL CANNULA receive FDA 510(k) clearance?
ARGYLE NASAL CANNULA received FDA 510(k) clearance on 1983-11-03, under 510(k) number K833127.
Who is the listed applicant for ARGYLE NASAL CANNULA?
The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARGYLE NASAL CANNULA?
The FDA product code for ARGYLE NASAL CANNULA is CAT.
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 Co. 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: CAT)
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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