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FDA 510(k)

MEDI-STIM, MODIFICATION

K-Number: K933237 · 1994-09-08

ApplicantMid-Canada Medical
Decision Date1994-09-08
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDI-STIM, MODIFICATION 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 1994-09-08 under 510(k) number K933237. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-STIM, MODIFICATION?

MEDI-STIM, MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-09-08. The listed applicant is Mid-Canada Medical. The 510(k) number is K933237.

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

MEDI-STIM, MODIFICATION received FDA 510(k) clearance on 1994-09-08, under 510(k) number K933237.

Who is the listed applicant for MEDI-STIM, MODIFICATION?

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, MODIFICATION?

The FDA product code for MEDI-STIM, MODIFICATION is GZJ.

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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.

K922839MID-CANADA MEDICALK921491MEDI-STIMK883309MULTI-CARE CHAIRK883308PARKER BATHING SYSTEM

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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