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FDA 510(k)

RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL

K-Number: K994387 · 2000-03-16

ApplicantWoodside Biomedical, Inc.
Decision Date2000-03-16
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL is the device name listed in this FDA 510(k) record. The listed applicant is Woodside Biomedical, Inc.. It received FDA 510(k) clearance on 2000-03-16 under 510(k) number K994387. 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 RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL?

RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL is a medical device that received FDA 510(k) clearance on 2000-03-16. The listed applicant is Woodside Biomedical, Inc.. The 510(k) number is K994387.

When did RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL receive FDA 510(k) clearance?

RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL received FDA 510(k) clearance on 2000-03-16, under 510(k) number K994387.

Who is the listed applicant for RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL?

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

What is the FDA product code for RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL?

The FDA product code for RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL 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 Woodside Biomedical, 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.

K020180RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RLK983907RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-RK982967RELIEFBAND MST DEVICE, MODELS RB-2, RB-6, RB-RK982436RELIEFBAND NST DEVICE, MODEL #'S WB-2, WB-6 AND WB-RK980333RELIEFBAND

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

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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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