Electronic Ultrasound Scan Models Eup-U12/012T/TC3

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

510(k) Number

K912363 ↗

FDA Product Code

ITX

Models / Variants

Eup-U12

012T

TC3

Device Class

Class II

Regulation

21 CFR Part 892.1570

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Eup-OL334 Laparascopicprobe

  Class II

  FDA 510(k) K981434 Active Cleared 27 Jul 1998

• Eup-V12 5.0 Mhz Convex Array Transvaginal Probe

  Class II

  FDA 510(k) K900966 Active Cleared 12 Sep 1990

• Eup-C321 5.0MHZ Convex Type Probe

  Class II

  FDA 510(k) K890532 Active Cleared 13 Apr 1990

• Eub-40

  Class II

  FDA 510(k) K844128 Active Cleared 25 Feb 1985

• Add'l Transducer for Use W/Eub-165 Ultrasound

  Class II

  FDA 510(k) K901658 Active Cleared 4 Sep 1990

• Eup-F124 5.0 Mhz Convex Array Finger Top Probe

  Class II

  FDA 510(k) K890531 Active Cleared 13 Apr 1990

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