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FDA 510(k)

MS-100 MYO-SCANNER OR MS-100 EMG SCANNER

K-Number: K921919 · 1993-01-07

Decision Date1993-01-07
Product CodeKZM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MS-100 MYO-SCANNER OR MS-100 EMG SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Myo-Tronics, Inc.. It received FDA 510(k) clearance on 1993-01-07 under 510(k) number K921919. The device is classified under product code KZM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MS-100 MYO-SCANNER OR MS-100 EMG SCANNER?

MS-100 MYO-SCANNER OR MS-100 EMG SCANNER is a medical device that received FDA 510(k) clearance on 1993-01-07. The listed applicant is Myo-Tronics, Inc.. The 510(k) number is K921919.

When did MS-100 MYO-SCANNER OR MS-100 EMG SCANNER receive FDA 510(k) clearance?

MS-100 MYO-SCANNER OR MS-100 EMG SCANNER received FDA 510(k) clearance on 1993-01-07, under 510(k) number K921919.

Who is the listed applicant for MS-100 MYO-SCANNER OR MS-100 EMG SCANNER?

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

What is the FDA product code for MS-100 MYO-SCANNER OR MS-100 EMG SCANNER?

The FDA product code for MS-100 MYO-SCANNER OR MS-100 EMG SCANNER is KZM.

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.

Other records listing Myo-Tronics, 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.

Related Devices (Code: KZM)

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.

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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