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FDA 510(k)

NERVTRON-RX

K-Number: K780444 · 1978-04-19

ApplicantMedix Corp.
Decision Date1978-04-19
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NERVTRON-RX is the device name listed in this FDA 510(k) record. The listed applicant is Medix Corp.. It received FDA 510(k) clearance on 1978-04-19 under 510(k) number K780444. 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 NERVTRON-RX?

NERVTRON-RX is a medical device that received FDA 510(k) clearance on 1978-04-19. The listed applicant is Medix Corp.. The 510(k) number is K780444.

When did NERVTRON-RX receive FDA 510(k) clearance?

NERVTRON-RX received FDA 510(k) clearance on 1978-04-19, under 510(k) number K780444.

Who is the listed applicant for NERVTRON-RX?

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

What is the FDA product code for NERVTRON-RX?

The FDA product code for NERVTRON-RX is GZJ.

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Other records listing Medix 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.

K921273EASIMIST ULTRASONIC NEBULIZERK914772MEDIX NEBULIZING SYSTEM CODE NO. 2000 AND 2001K853071MEDIX ELECTRONIC NEBULIZING SYSTEMK822454SYRINGE PUMP 209-100

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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