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FDA 510(k)

MYODAC2 BIOFEEDBACK DEVICE

K-Number: K894840 · 1989-10-13

ApplicantThought Technology , Ltd.
Decision Date1989-10-13
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MYODAC2 BIOFEEDBACK DEVICE 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 1989-10-13 under 510(k) number K894840. 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 MYODAC2 BIOFEEDBACK DEVICE?

MYODAC2 BIOFEEDBACK DEVICE is a medical device that received FDA 510(k) clearance on 1989-10-13. The listed applicant is Thought Technology , Ltd.. The 510(k) number is K894840.

When did MYODAC2 BIOFEEDBACK DEVICE receive FDA 510(k) clearance?

MYODAC2 BIOFEEDBACK DEVICE received FDA 510(k) clearance on 1989-10-13, under 510(k) number K894840.

Who is the listed applicant for MYODAC2 BIOFEEDBACK DEVICE?

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 MYODAC2 BIOFEEDBACK DEVICE?

The FDA product code for MYODAC2 BIOFEEDBACK DEVICE 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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