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)

SURX RF SYSTEM

K-Number: K020952 · 2002-05-30

ApplicantSurx, Inc.
Decision Date2002-05-30
Product CodeMUK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURX RF SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Surx, Inc.. It received FDA 510(k) clearance on 2002-05-30 under 510(k) number K020952. The device is classified under product code MUK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURX RF SYSTEM?

SURX RF SYSTEM is a medical device that received FDA 510(k) clearance on 2002-05-30. The listed applicant is Surx, Inc.. The 510(k) number is K020952.

When did SURX RF SYSTEM receive FDA 510(k) clearance?

SURX RF SYSTEM received FDA 510(k) clearance on 2002-05-30, under 510(k) number K020952.

Who is the listed applicant for SURX RF SYSTEM?

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

What is the FDA product code for SURX RF SYSTEM?

The FDA product code for SURX RF SYSTEM is MUK.

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 Surx, 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.

K020126MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM)K011190SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX LP SYSTEM)

Related Devices (Code: MUK)

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.

K020126MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM)Surx, Inc.K011190SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX LP SYSTEM)Surx, Inc.

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.

↑