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FDA 510(k)

TENS PRO 900

K-Number: K023726 · 2003-06-17

ApplicantAcumed Medical Supplies , Ltd.
Decision Date2003-06-17
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TENS PRO 900 is the device name listed in this FDA 510(k) record. The listed applicant is Acumed Medical Supplies , Ltd.. It received FDA 510(k) clearance on 2003-06-17 under 510(k) number K023726. 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 TENS PRO 900?

TENS PRO 900 is a medical device that received FDA 510(k) clearance on 2003-06-17. The listed applicant is Acumed Medical Supplies , Ltd.. The 510(k) number is K023726.

When did TENS PRO 900 receive FDA 510(k) clearance?

TENS PRO 900 received FDA 510(k) clearance on 2003-06-17, under 510(k) number K023726.

Who is the listed applicant for TENS PRO 900?

The FDA 510(k) record lists Acumed Medical Supplies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TENS PRO 900?

The FDA product code for TENS PRO 900 is GZJ.

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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