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FDA 510(k)

ELECTROTRACE, MODIFICATION

K-Number: K924133 · 1992-10-30

ApplicantJason Marketing Co.
Decision Date1992-10-30
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTROTRACE, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Jason Marketing Co.. It received FDA 510(k) clearance on 1992-10-30 under 510(k) number K924133. 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 ELECTROTRACE, MODIFICATION?

ELECTROTRACE, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-10-30. The listed applicant is Jason Marketing Co.. The 510(k) number is K924133.

When did ELECTROTRACE, MODIFICATION receive FDA 510(k) clearance?

ELECTROTRACE, MODIFICATION received FDA 510(k) clearance on 1992-10-30, under 510(k) number K924133.

Who is the listed applicant for ELECTROTRACE, MODIFICATION?

The FDA 510(k) record lists Jason Marketing Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROTRACE, MODIFICATION?

The FDA product code for ELECTROTRACE, MODIFICATION 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 Jason Marketing 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.

K903555ELECTROTRACE DISPOSABLE AG/AGCL EKG MON. ELEC.K896569ELECTROTRACE DISPOSABLE AG/AGCL EKG MONITOR ELEC.K894679ELECTROTRACE DISP. RESTING EKG ELECTRODESK871626ELECTROTRACE DISP REST EKG ELECTRODE, CAT. ET1200

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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