Skip to content

Rehcor

by Electromed Corp.

510(k) K990813

Rehcor is a Class II device made by Electromed Corp., cleared under FDA 510(k) K990813 on 12 Apr 1999, 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 NumberK990813 Date12 Apr 1999ClearedStatusActive

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  • Withdrawn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
ISD
Device class
Class II
Regulation
21 CFR Part 890.5360
Advisory committee
Physical Medicine
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code ISD (Exerciser, Measuring).

Other devices from Electromed, Inc.

See all devices from Electromed, Inc. →