Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NEUROTRAIN

K-Number: K883896 · 1989-07-14

ApplicantSterne Equipment Co., Ltd.
Decision Date1989-07-14
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROTRAIN is the device name listed in this FDA 510(k) record. The listed applicant is Sterne Equipment Co., Ltd.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K883896. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROTRAIN?

NEUROTRAIN is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Sterne Equipment Co., Ltd.. The 510(k) number is K883896.

When did NEUROTRAIN receive FDA 510(k) clearance?

NEUROTRAIN received FDA 510(k) clearance on 1989-07-14, under 510(k) number K883896.

Who is the listed applicant for NEUROTRAIN?

The FDA 510(k) record lists Sterne Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROTRAIN?

The FDA product code for NEUROTRAIN is LIH.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Sterne Equipment Co., Ltd. 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.

K003433NEURO-TRAIN III (3)K980158MYO-TRAIN V (5)K972204ACU-RAY HF SERIES PORTABLE X-RAY UNITK970155NEURO-TRAIN II (2)K931279ACU-RAY

Related Devices (Code: LIH)

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.

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLCK183692Avid IF2Vision Quest Industries Inc./Dba VQ OrthocareK122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLCK110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments Co.,Ltd

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.

↑