ARGYLE URINE METER
K-Number: K790969 · 1979-06-27
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Device Summary
Frequently Asked Questions
What is the ARGYLE URINE METER?
ARGYLE URINE METER is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is Sherwood Medical Co.. The 510(k) number is K790969.
When did ARGYLE URINE METER receive FDA 510(k) clearance?
ARGYLE URINE METER received FDA 510(k) clearance on 1979-06-27, under 510(k) number K790969.
Who is the listed applicant for ARGYLE URINE METER?
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 URINE METER?
The FDA product code for ARGYLE URINE METER 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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