FDA 510(k)

MEDI-STIM

K-Number: K921491 · 1992-09-03

Decision Date1992-09-03

Product CodeLIH

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MEDI-STIM is the device name listed in this FDA 510(k) record. The listed applicant is Mid-Canada Medical. It received FDA 510(k) clearance on 1992-09-03 under 510(k) number K921491. 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 MEDI-STIM?

MEDI-STIM is a medical device that received FDA 510(k) clearance on 1992-09-03. The listed applicant is Mid-Canada Medical. The 510(k) number is K921491.

When did MEDI-STIM receive FDA 510(k) clearance?

MEDI-STIM received FDA 510(k) clearance on 1992-09-03, under 510(k) number K921491.

Who is the listed applicant for MEDI-STIM?

The FDA 510(k) record lists Mid-Canada Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI-STIM?

The FDA product code for MEDI-STIM is LIH.

Other records listing Mid-Canada Medical 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.

K933237MEDI-STIM, MODIFICATION K922839MID-CANADA MEDICAL K883309MULTI-CARE CHAIR K883308PARKER BATHING SYSTEM

Related Devices (Code: LIH)

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLC K183692Avid IF2Vision Quest Industries Inc./Dba VQ Orthocare K122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLC K110509EVERYWAY 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.