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FDA 510(k)

NEU-PULS(TENS) MODEL #295

K-Number: K870583 · 1987-03-17

ApplicantOms Medico, Inc.
Decision Date1987-03-17
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEU-PULS(TENS) MODEL #295 is the device name listed in this FDA 510(k) record. The listed applicant is Oms Medico, Inc.. It received FDA 510(k) clearance on 1987-03-17 under 510(k) number K870583. 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 NEU-PULS(TENS) MODEL #295?

NEU-PULS(TENS) MODEL #295 is a medical device that received FDA 510(k) clearance on 1987-03-17. The listed applicant is Oms Medico, Inc.. The 510(k) number is K870583.

When did NEU-PULS(TENS) MODEL #295 receive FDA 510(k) clearance?

NEU-PULS(TENS) MODEL #295 received FDA 510(k) clearance on 1987-03-17, under 510(k) number K870583.

Who is the listed applicant for NEU-PULS(TENS) MODEL #295?

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

What is the FDA product code for NEU-PULS(TENS) MODEL #295?

The FDA product code for NEU-PULS(TENS) MODEL #295 is GZJ.

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Other records listing Oms Medico, Inc. 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.

K874550TX-4(TENS) (SIGMA TENS)K874333TX-2(TENS)K873420GLOBALCARE(TENS)K873484120Z(TENS)K871699TX-3(TENS)K865063UNI-PULS(TENS) MODEL #292

View all 7 devices →

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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