Telephonic Receiver R-10 EEG

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

510(k) Number

K833880 ↗

FDA Product Code

GYE

Device Class

Class II

Regulation

21 CFR Part 882.1855

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

• Adult Flexfloat

  Class I

  FDA 510(k) K812684 Active Cleared 8 Oct 1981

• Rodder Volume Ventilator

  Class II

  FDA 510(k) K820248 Active Cleared 16 Apr 1982

• Adult Flex Float W/Heater

  Class I

  FDA 510(k) K812681 Active Cleared 8 Oct 1981

• Home Blood Glucose Monitor

  Class II

  FDA 510(k) K822486 Active Cleared 5 Nov 1982

• Flexfloat Heater

  Class I

  FDA 510(k) K812682 Active Cleared 8 Oct 1981

• EEG Telephone Transmitter, Model #t-7

  Class II

  FDA 510(k) K813010 Active Cleared 16 Nov 1981

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