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FDA 510(k)

TENS MODEL 240Z

K-Number: K920266 · 1992-12-03

ApplicantOms Medical Supplies, Inc.
Decision Date1992-12-03
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TENS MODEL 240Z is the device name listed in this FDA 510(k) record. The listed applicant is Oms Medical Supplies, Inc.. It received FDA 510(k) clearance on 1992-12-03 under 510(k) number K920266. 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 MODEL 240Z?

TENS MODEL 240Z is a medical device that received FDA 510(k) clearance on 1992-12-03. The listed applicant is Oms Medical Supplies, Inc.. The 510(k) number is K920266.

When did TENS MODEL 240Z receive FDA 510(k) clearance?

TENS MODEL 240Z received FDA 510(k) clearance on 1992-12-03, under 510(k) number K920266.

Who is the listed applicant for TENS MODEL 240Z?

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

What is the FDA product code for TENS MODEL 240Z?

The FDA product code for TENS MODEL 240Z is GZJ.

Related Clinical Trials

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.

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Other records listing Oms Medical Supplies, 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.

K963194ITO ACUPUNCTURE NEEDLESK904388POINTER F-3 TENSK904332MSTIM-2000 EMSK894964K-2 TENS OR MED TENSK884210TX-7 (TENS) (IC-1107)

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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