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)

CONTOUR SOFT-E SERIES CONDUCTIVE SOLID GEL ELECTRO

K-Number: K871412 · 1987-05-12

ApplicantContour Electrodes, Inc.
Decision Date1987-05-12
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONTOUR SOFT-E SERIES CONDUCTIVE SOLID GEL ELECTRO is the device name listed in this FDA 510(k) record. The listed applicant is Contour Electrodes, Inc.. It received FDA 510(k) clearance on 1987-05-12 under 510(k) number K871412. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTOUR SOFT-E SERIES CONDUCTIVE SOLID GEL ELECTRO?

CONTOUR SOFT-E SERIES CONDUCTIVE SOLID GEL ELECTRO is a medical device that received FDA 510(k) clearance on 1987-05-12. The listed applicant is Contour Electrodes, Inc.. The 510(k) number is K871412.

When did CONTOUR SOFT-E SERIES CONDUCTIVE SOLID GEL ELECTRO receive FDA 510(k) clearance?

CONTOUR SOFT-E SERIES CONDUCTIVE SOLID GEL ELECTRO received FDA 510(k) clearance on 1987-05-12, under 510(k) number K871412.

Who is the listed applicant for CONTOUR SOFT-E SERIES CONDUCTIVE SOLID GEL ELECTRO?

The FDA 510(k) record lists Contour Electrodes, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTOUR SOFT-E SERIES CONDUCTIVE SOLID GEL ELECTRO?

The FDA product code for CONTOUR SOFT-E SERIES CONDUCTIVE SOLID GEL ELECTRO is DRX.

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 Contour Electrodes, 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.

K900682PHANTOM RADIOTRANSLUCENT ECG MONITORING ELECTRODEK893245L30-LB- INFANT LIMB BANDK881085SOFT-E SERIES T-10 ACCUTRACE TAB RESTING ELECTRODE

Related Devices (Code: DRX)

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.

K171244PhysiotraceNimbleheart, Inc.K123658BIOMODULE 3-M1Zephyr Technology CorporationK101576CENTERRIDGE DIAGNOSTIC ECG ELECTRODE, CENTERRIDGE MONITORING ECG ELECTRODESTeam Innovations, Inc.K101685IP-SETIntegral Process SasK100129AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO XAmbu A/SK093327INTCO TAB ELECTRODEShanghai Intco Electrode Manufacturing Co., Ltd.

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.

↑