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FDA 510(k)

MYOTRAC+/S, MYODAC+/S

K-Number: K913898 · 1992-03-26

ApplicantThought Technology , Ltd.
Decision Date1992-03-26
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MYOTRAC+/S, MYODAC+/S is the device name listed in this FDA 510(k) record. The listed applicant is Thought Technology , Ltd.. It received FDA 510(k) clearance on 1992-03-26 under 510(k) number K913898. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYOTRAC+/S, MYODAC+/S?

MYOTRAC+/S, MYODAC+/S is a medical device that received FDA 510(k) clearance on 1992-03-26. The listed applicant is Thought Technology , Ltd.. The 510(k) number is K913898.

When did MYOTRAC+/S, MYODAC+/S receive FDA 510(k) clearance?

MYOTRAC+/S, MYODAC+/S received FDA 510(k) clearance on 1992-03-26, under 510(k) number K913898.

Who is the listed applicant for MYOTRAC+/S, MYODAC+/S?

The FDA 510(k) record lists Thought Technology , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MYOTRAC+/S, MYODAC+/S?

The FDA product code for MYOTRAC+/S, MYODAC+/S is HCC.

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Other records listing Thought Technology , Ltd. as applicant

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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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