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FDA 510(k)

MEDS-3 NEUROMUSCULAR STIMULATOR

K-Number: K023443 · 2003-01-13

ApplicantMedical Equipment Device Specialists
Decision Date2003-01-13
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDS-3 NEUROMUSCULAR STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Device Specialists. It received FDA 510(k) clearance on 2003-01-13 under 510(k) number K023443. 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 MEDS-3 NEUROMUSCULAR STIMULATOR?

MEDS-3 NEUROMUSCULAR STIMULATOR is a medical device that received FDA 510(k) clearance on 2003-01-13. The listed applicant is Medical Equipment Device Specialists. The 510(k) number is K023443.

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

MEDS-3 NEUROMUSCULAR STIMULATOR received FDA 510(k) clearance on 2003-01-13, under 510(k) number K023443.

Who is the listed applicant for MEDS-3 NEUROMUSCULAR STIMULATOR?

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

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

The FDA product code for MEDS-3 NEUROMUSCULAR STIMULATOR is GZJ.

Related Clinical Trials

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Other records listing Medical Equipment Device Specialists 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.

K040193MODEL GST-1K032055MEDS-4-INF+K023439MEDS-4 NEUROMUSCULAR STIMULATORK023446MEDS-3 NEUROMUSCULAR STIMULATORK023435MEDS-4 NEUROMUSCULAR STIMULATOR

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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