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)

MEDRELIEF

K-Number: K003507 · 2001-02-21

ApplicantHealthonics, Inc.
Decision Date2001-02-21
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDRELIEF is the device name listed in this FDA 510(k) record. The listed applicant is Healthonics, Inc.. It received FDA 510(k) clearance on 2001-02-21 under 510(k) number K003507. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDRELIEF?

MEDRELIEF is a medical device that received FDA 510(k) clearance on 2001-02-21. The listed applicant is Healthonics, Inc.. The 510(k) number is K003507.

When did MEDRELIEF receive FDA 510(k) clearance?

MEDRELIEF received FDA 510(k) clearance on 2001-02-21, under 510(k) number K003507.

Who is the listed applicant for MEDRELIEF?

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

What is the FDA product code for MEDRELIEF?

The FDA product code for MEDRELIEF is GZJ.

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 Healthonics, 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.

K060669MEDRELIEF ST SERIES, MODELS RT-50, ST-100, ST 150, ST-200, ST-300K030998MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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.

↑