Telephone Receivers R101 R111

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K840032 ↗

FDA Product Code

DXH

Device Class

Class II

Regulation

21 CFR Part 870.2920

Advisory Committee

Cardiovascular

FDA Decision

SESP Substantially Equivalent — Postmarket Surveillance

• Model T131 Memory Transmitter

  Class II

  FDA 510(k) K933021 Active Cleared 6 Jun 1994

• Model Mc-1 Surgical Video Camera

  Class I

  FDA 510(k) K863376 Active Cleared 2 Oct 1986

• Memory Loop Transmitter #121

  Class II

  FDA 510(k) K832951 Active Cleared 17 Feb 1984

• Model T 101 Clinical Transmitter

  Class II

  FDA 510(k) K842435 Active Cleared 16 May 1985