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)

INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2

K-Number: K921612 · 1992-08-18

ApplicantMedstar, Inc.
Decision Date1992-08-18
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2 is the device name listed in this FDA 510(k) record. The listed applicant is Medstar, Inc.. It received FDA 510(k) clearance on 1992-08-18 under 510(k) number K921612. 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 INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2?

INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2 is a medical device that received FDA 510(k) clearance on 1992-08-18. The listed applicant is Medstar, Inc.. The 510(k) number is K921612.

When did INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2 receive FDA 510(k) clearance?

INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2 received FDA 510(k) clearance on 1992-08-18, under 510(k) number K921612.

Who is the listed applicant for INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2?

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

What is the FDA product code for INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2?

The FDA product code for INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2 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 Medstar, 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.

K880548SAFE-STRIPS

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.

↑