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FDA 510(k)

NSD 8CS8 - TENS DEVICE

K-Number: K892408 · 1989-06-23

ApplicantFuture Medical Products, Inc.
Decision Date1989-06-23
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NSD 8CS8 - TENS DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Future Medical Products, Inc.. It received FDA 510(k) clearance on 1989-06-23 under 510(k) number K892408. 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 NSD 8CS8 - TENS DEVICE?

NSD 8CS8 - TENS DEVICE is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Future Medical Products, Inc.. The 510(k) number is K892408.

When did NSD 8CS8 - TENS DEVICE receive FDA 510(k) clearance?

NSD 8CS8 - TENS DEVICE received FDA 510(k) clearance on 1989-06-23, under 510(k) number K892408.

Who is the listed applicant for NSD 8CS8 - TENS DEVICE?

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

What is the FDA product code for NSD 8CS8 - TENS DEVICE?

The FDA product code for NSD 8CS8 - 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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