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Micropad

by Fia Man Co. 510(k)

Active United States

510(k) K823301

Overview

At Fia Man Co., we are proud to introduce the MICROPAD, a state-of-the-art physical medicine device designed to provide reliable and efficient pain management. With its innovative features and cutting-edge technology, this device has been deemed substantially equivalent to industry standards, meeting or exceeding all relevant regulatory requirements.

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK823301 Date3 Dec 1982ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
IRT
Device Class
Class II
Regulation
21 CFR Part 890.5740
Advisory Committee
Physical Medicine
FDA Decision
SESE Substantially Equivalent