URINE TESTER, MODEL NO. 707
K-Number: K770423 · 1977-06-03
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Device Summary
Frequently Asked Questions
What is the URINE TESTER, MODEL NO. 707?
URINE TESTER, MODEL NO. 707 is a medical device that received FDA 510(k) clearance on 1977-06-03. The listed applicant is Brother Scientific Products, Inc.. The 510(k) number is K770423.
When did URINE TESTER, MODEL NO. 707 receive FDA 510(k) clearance?
URINE TESTER, MODEL NO. 707 received FDA 510(k) clearance on 1977-06-03, under 510(k) number K770423.
Who is the listed applicant for URINE TESTER, MODEL NO. 707?
The FDA 510(k) record lists Brother Scientific Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URINE TESTER, MODEL NO. 707?
The FDA product code for URINE TESTER, MODEL NO. 707 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 Brother Scientific Products, Inc. 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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