Reliance Model 200 Podiatry Chair

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K860519 ↗

FDA Product Code

LGX

Device Class

Class I

Regulation

21 CFR Part 878.4960

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Reliance Tempo Ophth. Instr Stand

  Class I

  FDA 510(k) K831568 Active Cleared 30 Jun 1983

• Reliance Ophthalmic Slit Lamp R-083

  Class II

  FDA 510(k) K834060 Active Cleared 4 Feb 1984

• Reliance 6100

  Class I

  FDA 510(k) K853150 Active Cleared 5 Sep 1985

• Reliance Ophthalmic Instrument Control

  Class I

  FDA 510(k) K812544 Active Cleared 21 Sep 1981

• Reliance 5000

  Class I

  FDA 510(k) K853151 Active Cleared 5 Sep 1985

• Reliance Mod-U-Line M-700

  Class II

  FDA 510(k) K761147 Active Cleared 28 Jan 1977

See all devices from F. & F. Koenigkramer →