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FDA 510(k)

HMS-DHR-3 NEUROMUSCULAR STIMULATOR

K-Number: K021496 · 2002-08-06

ApplicantHome Medical Services
Decision Date2002-08-06
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HMS-DHR-3 NEUROMUSCULAR STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Home Medical Services. It received FDA 510(k) clearance on 2002-08-06 under 510(k) number K021496. 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 HMS-DHR-3 NEUROMUSCULAR STIMULATOR?

HMS-DHR-3 NEUROMUSCULAR STIMULATOR is a medical device that received FDA 510(k) clearance on 2002-08-06. The listed applicant is Home Medical Services. The 510(k) number is K021496.

When did HMS-DHR-3 NEUROMUSCULAR STIMULATOR receive FDA 510(k) clearance?

HMS-DHR-3 NEUROMUSCULAR STIMULATOR received FDA 510(k) clearance on 2002-08-06, under 510(k) number K021496.

Who is the listed applicant for HMS-DHR-3 NEUROMUSCULAR STIMULATOR?

The FDA 510(k) record lists Home Medical Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HMS-DHR-3 NEUROMUSCULAR STIMULATOR?

The FDA product code for HMS-DHR-3 NEUROMUSCULAR STIMULATOR 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 Home Medical Services 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.

K021472HMS-DHR-3 NEUROMUSCULAR STIMULATORK003231HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3

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.

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