ARGYLE CONNECT TUBE-CON & NON
K-Number: K802777 · 1980-12-11
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Device Summary
Frequently Asked Questions
What is the ARGYLE CONNECT TUBE-CON & NON?
ARGYLE CONNECT TUBE-CON & NON is a medical device that received FDA 510(k) clearance on 1980-12-11. The listed applicant is Sherwood Medical Co.. The 510(k) number is K802777.
When did ARGYLE CONNECT TUBE-CON & NON receive FDA 510(k) clearance?
ARGYLE CONNECT TUBE-CON & NON received FDA 510(k) clearance on 1980-12-11, under 510(k) number K802777.
Who is the listed applicant for ARGYLE CONNECT TUBE-CON & NON?
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 CONNECT TUBE-CON & NON?
The FDA product code for ARGYLE CONNECT TUBE-CON & NON is GAZ.
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: GAZ)
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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