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FDA 510(k)

MATRIX PRO-ELECDT

K-Number: K930263 · 1994-06-09

ApplicantMatrix Electromedical, Inc.
Decision Date1994-06-09
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MATRIX PRO-ELECDT 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 1994-06-09 under 510(k) number K930263. 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 PRO-ELECDT?

MATRIX PRO-ELECDT is a medical device that received FDA 510(k) clearance on 1994-06-09. The listed applicant is Matrix Electromedical, Inc.. The 510(k) number is K930263.

When did MATRIX PRO-ELECDT receive FDA 510(k) clearance?

MATRIX PRO-ELECDT received FDA 510(k) clearance on 1994-06-09, under 510(k) number K930263.

Who is the listed applicant for MATRIX PRO-ELECDT?

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 PRO-ELECDT?

The FDA product code for MATRIX PRO-ELECDT 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.

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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.

K930264MATRIX ELECDT & VACUPULLS

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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