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FDA 510(k)

S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR

K-Number: K033253 · 2003-10-21

ApplicantMicro Current Technology, Inc.
Decision Date2003-10-21
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Micro Current Technology, Inc.. It received FDA 510(k) clearance on 2003-10-21 under 510(k) number K033253. 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 S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR?

S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR is a medical device that received FDA 510(k) clearance on 2003-10-21. The listed applicant is Micro Current Technology, Inc.. The 510(k) number is K033253.

When did S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR receive FDA 510(k) clearance?

S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR received FDA 510(k) clearance on 2003-10-21, under 510(k) number K033253.

Who is the listed applicant for S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR?

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

What is the FDA product code for S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR?

The FDA product code for S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR is GZJ.

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Other records listing Micro Current Technology, Inc. as applicant

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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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