Esophogeal Ph Catheter

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

510(k) Number

K850074 ↗

FDA Product Code

FFT

Device Class

Class I

Regulation

21 CFR Part 876.1400

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K903662 Active Cleared 12 Dec 1990

• Islami Gastrointestinal Tube

  Class II

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  Class II

  FDA 510(k) K051480 Active Cleared 12 Oct 2005

• Ambi-24 Ph/Pressure Monitor

  Class I

  FDA 510(k) K854514 Active Cleared 24 Feb 1986

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