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FDA 510(k)

SCRAMBLER ST 5 TENS DEVICE

K-Number: K081255 · 2009-02-20

ApplicantCompetitive Technologies,Inc.
Decision Date2009-02-20
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SCRAMBLER ST 5 TENS DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Competitive Technologies,Inc.. It received FDA 510(k) clearance on 2009-02-20 under 510(k) number K081255. 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 SCRAMBLER ST 5 TENS DEVICE?

SCRAMBLER ST 5 TENS DEVICE is a medical device that received FDA 510(k) clearance on 2009-02-20. The listed applicant is Competitive Technologies,Inc.. The 510(k) number is K081255.

When did SCRAMBLER ST 5 TENS DEVICE receive FDA 510(k) clearance?

SCRAMBLER ST 5 TENS DEVICE received FDA 510(k) clearance on 2009-02-20, under 510(k) number K081255.

Who is the listed applicant for SCRAMBLER ST 5 TENS DEVICE?

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

What is the FDA product code for SCRAMBLER ST 5 TENS DEVICE?

The FDA product code for SCRAMBLER ST 5 TENS DEVICE is GZJ.

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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

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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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