DOVER URINE METER
K-Number: K771561 · 1977-09-07
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Device Summary
Frequently Asked Questions
What is the DOVER URINE METER?
DOVER URINE METER is a medical device that received FDA 510(k) clearance on 1977-09-07. The listed applicant is Will Ross Co.. The 510(k) number is K771561.
When did DOVER URINE METER receive FDA 510(k) clearance?
DOVER URINE METER received FDA 510(k) clearance on 1977-09-07, under 510(k) number K771561.
Who is the listed applicant for DOVER URINE METER?
The FDA 510(k) record lists Will Ross Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DOVER URINE METER?
The FDA product code for DOVER URINE METER is EXR.
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 Will Ross 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: EXR)
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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