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FDA 510(k)

MEC-I-TRON MINI, MODEL M-2

K-Number: K895289 · 1990-01-19

ApplicantMeyer Equipment Company, Inc.
Decision Date1990-01-19
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEC-I-TRON MINI, MODEL M-2 is the device name listed in this FDA 510(k) record. The listed applicant is Meyer Equipment Company, Inc.. It received FDA 510(k) clearance on 1990-01-19 under 510(k) number K895289. 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 MEC-I-TRON MINI, MODEL M-2?

MEC-I-TRON MINI, MODEL M-2 is a medical device that received FDA 510(k) clearance on 1990-01-19. The listed applicant is Meyer Equipment Company, Inc.. The 510(k) number is K895289.

When did MEC-I-TRON MINI, MODEL M-2 receive FDA 510(k) clearance?

MEC-I-TRON MINI, MODEL M-2 received FDA 510(k) clearance on 1990-01-19, under 510(k) number K895289.

Who is the listed applicant for MEC-I-TRON MINI, MODEL M-2?

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

What is the FDA product code for MEC-I-TRON MINI, MODEL M-2?

The FDA product code for MEC-I-TRON MINI, MODEL M-2 is GZJ.

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 Meyer Equipment Company, 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.

K873190MEC-I-TRON, MODEL P-1

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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