MS-100 MYO-SCANNER OR MS-100 EMG SCANNER
K-Number: K921919 · 1993-01-07
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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