FDA 510(k)

DS-200 AND DS-400 T.E.N.S.

K-Number: K881832 · 1988-07-01

Decision Date1988-07-01

Product CodeGZJ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

DS-200 AND DS-400 T.E.N.S. is the device name listed in this FDA 510(k) record. The listed applicant is Delta Marketing, Inc.. It received FDA 510(k) clearance on 1988-07-01 under 510(k) number K881832. 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 DS-200 AND DS-400 T.E.N.S.?

DS-200 AND DS-400 T.E.N.S. is a medical device that received FDA 510(k) clearance on 1988-07-01. The listed applicant is Delta Marketing, Inc.. The 510(k) number is K881832.

When did DS-200 AND DS-400 T.E.N.S. receive FDA 510(k) clearance?

DS-200 AND DS-400 T.E.N.S. received FDA 510(k) clearance on 1988-07-01, under 510(k) number K881832.

Who is the listed applicant for DS-200 AND DS-400 T.E.N.S.?

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

What is the FDA product code for DS-200 AND DS-400 T.E.N.S.?

The FDA product code for DS-200 AND DS-400 T.E.N.S. 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 miniSublimed K252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLC K232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical Officer K233046Electrical 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.