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Myodac

by Thought Technology Ltd.

510(k) K883597

Myodac is a Class II device made by Thought Technology Ltd., cleared under FDA 510(k) K883597 on 16 Nov 1988, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK883597 Date16 Nov 1988ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
HCC
FDA applicant
Thought Technology , Ltd.
Device class
Class II
Regulation
21 CFR Part 882.5050
Advisory committee
Neurology
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code HCC (Device, Biofeedback).

Other devices from Thought Technology Ltd.

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