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FDA 510(k)

RADX SYSTEM

K-Number: K965203 · 1997-03-17

ApplicantElectro Medical Systems, Inc.
Decision Date1997-03-17
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RADX SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Electro Medical Systems, Inc.. It received FDA 510(k) clearance on 1997-03-17 under 510(k) number K965203. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADX SYSTEM?

RADX SYSTEM is a medical device that received FDA 510(k) clearance on 1997-03-17. The listed applicant is Electro Medical Systems, Inc.. The 510(k) number is K965203.

When did RADX SYSTEM receive FDA 510(k) clearance?

RADX SYSTEM received FDA 510(k) clearance on 1997-03-17, under 510(k) number K965203.

Who is the listed applicant for RADX SYSTEM?

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

What is the FDA product code for RADX SYSTEM?

The FDA product code for RADX SYSTEM is EHD.

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 Electro Medical Systems, 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.

K991857AIRFLOW HANDY

Related Devices (Code: EHD)

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.

K260795Hand-held Dental X-ray System (HyperLight-M)Changzhou Sifary Medical Technology Co., Ltd.K260367Portable Dental X-ray System Model PDX novaPDX Co., Ltd.K253864NOMAD Pro 3Dental Imaging Technologies CorporationK252110Dental X-RAY Unit (AJX200)Guangzhou Ajax Medical Equipment Co., Ltd.K254018Portable Dental X-ray Device (GT-1)Guilin Refine Medical Instrument Co., Ltd.K252909Diagnostic X-Ray Equipment Model POCT22Ningbo Runyes Medical Instrument 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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