Browne Model Ud-4D

No FDA recalls on record, checked 9 Oct 2026.

510(k) Number

K792091 ↗

FDA Product Code

FAP

Device Class

Class II

Regulation

21 CFR Part 876.1620

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Browne Model Cf-1 and Cf-1g

  Class II

  FDA 510(k) K790754 Active Cleared 1 Jun 1979

• Browne Model Ua-6

  Class II

  FDA 510(k) K792094 Active Cleared 6 Dec 1979

• Browne Model Gd-5

  Class II

  FDA 510(k) K792093 Active Cleared 6 Dec 1979

• Browne Model UD-4DE

  Class II

  FDA 510(k) K790478 Active Cleared 1 Jun 1979

• Browne Model Ud-4

  Class II

  FDA 510(k) K792090 Active Cleared 6 Dec 1979

• Browne Model Ud-4E

  Class II

  FDA 510(k) K792092 Active Cleared 6 Dec 1979