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Acuson V714 Transducer

by Acuson Corp.

510(k) K920882

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK920882 Date26 Mar 1993ClearedStatusActive

Recalls

0 recalls · FDA

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

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
ITX
Device Class
Class II
Regulation
21 CFR Part 892.1570
Advisory Committee
Radiology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 25 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The ACUSON V714 TRANSDUCER is a diagnostic ultrasound transducer classified under product code ITX as a Transducer, Ultrasonic, Diagnostic. It is a Class II medical device subject to special controls, as determined by its FDA 510(k) clearance.

The device was cleared via the traditional 510(k) pathway under K920882, with a decision date of March 26, 1993, and is manufactured by Acuson Corp. in Mountain View, California. It is intended for use in radiology settings as indicated by the advisory committee classification.

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Questions

AI-generated answers, 25 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the ACUSON V714 TRANSDUCER used for?

    The ACUSON V714 TRANSDUCER is a diagnostic ultrasound transducer intended for use in radiology settings, as indicated by its advisory committee classification under product code ITX for ultrasonic diagnostic transducers.

  • How was the ACUSON V714 TRANSDUCER cleared for market?

    The device was cleared via the traditional FDA 510(k) pathway under submission K920882, with a decision of substantially equivalent granted on March 26, 1993, based on its classification as a Class II medical device.

  • Who manufactures the ACUSON V714 TRANSDUCER and where is it made?

    The ACUSON V714 TRANSDUCER is manufactured by Acuson Corp. at their facility located at 1220 Charleston Rd., Mountain View, California, 94039, United States.