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FDA 510(k)

FOCUS MODEL 795 UNIT

K-Number: K951951 · 1996-05-17

ApplicantEmpi
Decision Date1996-05-17
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

FOCUS MODEL 795 UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Empi. It received FDA 510(k) clearance on 1996-05-17 under 510(k) number K951951. 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 FOCUS MODEL 795 UNIT?

FOCUS MODEL 795 UNIT is a medical device that received FDA 510(k) clearance on 1996-05-17. The listed applicant is Empi. The 510(k) number is K951951.

When did FOCUS MODEL 795 UNIT receive FDA 510(k) clearance?

FOCUS MODEL 795 UNIT received FDA 510(k) clearance on 1996-05-17, under 510(k) number K951951.

Who is the listed applicant for FOCUS MODEL 795 UNIT?

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

What is the FDA product code for FOCUS MODEL 795 UNIT?

The FDA product code for FOCUS MODEL 795 UNIT is GZJ.

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Other records listing Empi 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.

K093324EMPI CONTINUUMK090922EMPI ACTIVE TRANSCUTANEOUS NERVE STIMULATORK072946HYBRESIS IONTOPHORESIS DRUG DELIVERY SYSTEMK070427DUPEL TRANSPORT IONTOPHORESIS SYSTEMK061650SELECT TENS, MODEL 4600SK041920INFINITY PLUS ELECTROTHERAPY SYSTEM

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Related Devices (Code: GZJ)

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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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