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FDA 510(k)

MYOTONE EMG MONITOR

K-Number: K772005 · 1977-11-23

ApplicantMicro Tronics Corp.
Decision Date1977-11-23
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MYOTONE EMG MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Micro Tronics Corp.. It received FDA 510(k) clearance on 1977-11-23 under 510(k) number K772005. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYOTONE EMG MONITOR?

MYOTONE EMG MONITOR is a medical device that received FDA 510(k) clearance on 1977-11-23. The listed applicant is Micro Tronics Corp.. The 510(k) number is K772005.

When did MYOTONE EMG MONITOR receive FDA 510(k) clearance?

MYOTONE EMG MONITOR received FDA 510(k) clearance on 1977-11-23, under 510(k) number K772005.

Who is the listed applicant for MYOTONE EMG MONITOR?

The FDA 510(k) record lists Micro Tronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MYOTONE EMG MONITOR?

The FDA product code for MYOTONE EMG MONITOR is IKN.

Related Clinical Trials

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Other records listing Micro Tronics Corp. 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.

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Related Devices (Code: IKN)

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.

K172743Natus VikingQuestNatus Neurology IncorporatedK163150ViMove2Dorsavi, Ltd.K162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.K123902PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)Oktx, LLCK123399MYOVISION 3.0 WIREFREE SYSTEMPrecision Biometrics, Inc.K113074CMAP PROMedical Technologies, Inc.

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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