Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

URINE TESTER, MODEL 701

K-Number: K770939 · 1977-06-03

ApplicantBrother Scientific Products, Inc.
Decision Date1977-06-03
Product CodeEXR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URINE TESTER, MODEL 701 is the device name listed in this FDA 510(k) record. The listed applicant is Brother Scientific Products, Inc.. It received FDA 510(k) clearance on 1977-06-03 under 510(k) number K770939. The device is classified under product code EXR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINE TESTER, MODEL 701?

URINE TESTER, MODEL 701 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 K770939.

When did URINE TESTER, MODEL 701 receive FDA 510(k) clearance?

URINE TESTER, MODEL 701 received FDA 510(k) clearance on 1977-06-03, under 510(k) number K770939.

Who is the listed applicant for URINE TESTER, MODEL 701?

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 701?

The FDA product code for URINE TESTER, MODEL 701 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K770423URINE TESTER, MODEL NO. 707

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.

K934142URINARY DRAINAGE BAGKey Medical Services, Inc.K935578URINE METERPuritas Health Care, Inc.K911258KENDALL PEDIATRIC URINE METERKendall Healthcare Products Co. Div.Of Tyco HealthK896732UNOMETER 500Unoplast A/SK870240COMPRESS AND SKULLCAP, HEAD DRESSINGFraass Survival Systems, Inc.K771561DOVER URINE METERWill Ross Co.

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.

↑