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FDA 510(k)

MODEL 402P SEQUENCER FOR EMPI TEMS DEV

K-Number: K823299 · 1982-12-15

ApplicantEpmi, Inc.
Decision Date1982-12-15
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL 402P SEQUENCER FOR EMPI TEMS DEV is the device name listed in this FDA 510(k) record. The listed applicant is Epmi, Inc.. It received FDA 510(k) clearance on 1982-12-15 under 510(k) number K823299. 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 MODEL 402P SEQUENCER FOR EMPI TEMS DEV?

MODEL 402P SEQUENCER FOR EMPI TEMS DEV is a medical device that received FDA 510(k) clearance on 1982-12-15. The listed applicant is Epmi, Inc.. The 510(k) number is K823299.

When did MODEL 402P SEQUENCER FOR EMPI TEMS DEV receive FDA 510(k) clearance?

MODEL 402P SEQUENCER FOR EMPI TEMS DEV received FDA 510(k) clearance on 1982-12-15, under 510(k) number K823299.

Who is the listed applicant for MODEL 402P SEQUENCER FOR EMPI TEMS DEV?

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

What is the FDA product code for MODEL 402P SEQUENCER FOR EMPI TEMS DEV?

The FDA product code for MODEL 402P SEQUENCER FOR EMPI TEMS DEV 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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