Phoresor Model PM2000

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K001410 ↗

FDA Product Code

KTB

Device Class

Class II

Regulation

21 CFR Part 890.5525

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Phoresor II, Model PM900

  Class II

  FDA 510(k) K974855 Active Cleared 27 Mar 1998

• Phoresor II Auto, Model PM800 Modification

  Class II

  FDA 510(k) K934335 Active Cleared 26 Jul 1994

• Transq 2

  Class II

  FDA 510(k) K914264 Active Cleared 20 Dec 1991

• Champion Iontophoretic Drug Delivery Device

  Class II

  FDA 510(k) K063465 Active Cleared 28 Feb 2007

• Rh-801/Gs Model Transq(R)1

  Class II

  FDA 510(k) K932621 Active Cleared 26 Jul 1994

• Rh-806, Model Transq

  Class II

  FDA 510(k) K925800 Active Cleared 14 Jul 1994

See all devices from Iomed, Inc. →