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)

MATRIX ELECDT & VACUPULLS

K-Number: K930264 · 1993-06-29

ApplicantMatrix Electromedical, Inc.
Decision Date1993-06-29
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MATRIX ELECDT & VACUPULLS is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Electromedical, Inc.. It received FDA 510(k) clearance on 1993-06-29 under 510(k) number K930264. 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 MATRIX ELECDT & VACUPULLS?

MATRIX ELECDT & VACUPULLS is a medical device that received FDA 510(k) clearance on 1993-06-29. The listed applicant is Matrix Electromedical, Inc.. The 510(k) number is K930264.

When did MATRIX ELECDT & VACUPULLS receive FDA 510(k) clearance?

MATRIX ELECDT & VACUPULLS received FDA 510(k) clearance on 1993-06-29, under 510(k) number K930264.

Who is the listed applicant for MATRIX ELECDT & VACUPULLS?

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

What is the FDA product code for MATRIX ELECDT & VACUPULLS?

The FDA product code for MATRIX ELECDT & VACUPULLS 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 Matrix Electromedical, 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.

K930263MATRIX PRO-ELECDT

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.

↑