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FDA 510(k)

TENS DEVICE FOR RELIEF OF CHRONIC PAIN

K-Number: K864114 · 1987-04-01

ApplicantFuturemed Div. of Future Impex Corp.
Decision Date1987-04-01
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TENS DEVICE FOR RELIEF OF CHRONIC PAIN is the device name listed in this FDA 510(k) record. The listed applicant is Futuremed Div. of Future Impex Corp.. It received FDA 510(k) clearance on 1987-04-01 under 510(k) number K864114. 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 DEVICE FOR RELIEF OF CHRONIC PAIN?

TENS DEVICE FOR RELIEF OF CHRONIC PAIN is a medical device that received FDA 510(k) clearance on 1987-04-01. The listed applicant is Futuremed Div. of Future Impex Corp.. The 510(k) number is K864114.

When did TENS DEVICE FOR RELIEF OF CHRONIC PAIN receive FDA 510(k) clearance?

TENS DEVICE FOR RELIEF OF CHRONIC PAIN received FDA 510(k) clearance on 1987-04-01, under 510(k) number K864114.

Who is the listed applicant for TENS DEVICE FOR RELIEF OF CHRONIC PAIN?

The FDA 510(k) record lists Futuremed Div. of Future Impex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TENS DEVICE FOR RELIEF OF CHRONIC PAIN?

The FDA product code for TENS DEVICE FOR RELIEF OF CHRONIC PAIN is GZJ.

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Other records listing Futuremed Div. of Future Impex Corp. as applicant

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.

K933511UPGRADED SPIROMETER ST-90K933220SELECTOR SL 01K933222AUDIOMETER DA 323K903017MEGA-TENS DUAL CHANNEL T.E.N.S.K901308SPIRO ANALYZER MODEL ST 250K884972TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR

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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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