ARGYLE CLOSED URINARY DRAINAGE SET
K-Number: K802667 · 1980-12-16
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Device Summary
Frequently Asked Questions
What is the ARGYLE CLOSED URINARY DRAINAGE SET?
ARGYLE CLOSED URINARY DRAINAGE SET is a medical device that received FDA 510(k) clearance on 1980-12-16. The listed applicant is Sherwood Medical Co.. The 510(k) number is K802667.
When did ARGYLE CLOSED URINARY DRAINAGE SET receive FDA 510(k) clearance?
ARGYLE CLOSED URINARY DRAINAGE SET received FDA 510(k) clearance on 1980-12-16, under 510(k) number K802667.
Who is the listed applicant for ARGYLE CLOSED URINARY DRAINAGE SET?
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 CLOSED URINARY DRAINAGE SET?
The FDA product code for ARGYLE CLOSED URINARY DRAINAGE SET is KNX.
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: KNX)
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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