Electrode Impedance Tester-Model 500

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K781475 ↗

FDA Product Code

GYA

Device Class

Class I

Regulation

21 CFR Part 882.1410

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

• Model 7320 Visual Stimulator

  Class II

  FDA 510(k) K781461 Active Cleared 8 Nov 1978

• Mular Gold Leaf Electrode Model 7501

  Class II

  FDA 510(k) K781476 Active Cleared 15 Nov 1978

• Preamplifier Models 8101PI & 8102PI

  Class II

  FDA 510(k) K781474 Active Cleared 7 Sep 1978

• Ear Electrode-Adult & Pediatric

  Class II

  FDA 510(k) K780537 Active Cleared 2 Jun 1978

• Audio Monitor-Model 8309

  Class II

  FDA 510(k) K780538 Active Cleared 19 Apr 1978

• Urodynamic Instruments

  Class II

  FDA 510(k) K770897 Active Cleared 3 Jun 1977

See all devices from Life-Tech Instruments, Inc. →