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Model Mi 44 Tympanometer

by Maico-Diagnostics

510(k) K060885

Model Mi 44 Tympanometer is a Class II device made by Maico-Diagnostics, cleared under FDA 510(k) K060885 on 5 Jun 2006, 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 NumberK060885 Date5 Jun 2006ClearedStatusActive

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  • Withdrawn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
EWO
Device class
Class II
Regulation
21 CFR Part 874.1050
Advisory committee
Ear, Nose, Throat
FDA decision
SESE Substantially Equivalent

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