Acuson S519 Transducer

FDA 510(k) K861596 · Acuson Computed Sonography

Substantially Equivalent for Some Indications

510(k) numberK861596

Submission

Device name
Acuson S519 Transducer
Applicant
Acuson Computed Sonography
Mountain View, CA, US
Received
April 29, 1986
Decision date
July 30, 1986
Decision
Substantially Equivalent for Some Indications (SN)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JOP – Transducer, Ultrasonic
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2880
Specialty
Cardiovascular

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More from Echocath, Inc.

510(k)DeviceDecision
K893863Acuson L538 TransducerITX · Traditional 05/23/1990SE
K874028Acuson S328 TransducerIYO · Traditional 06/21/1988SE
K874861Acuson S328 Transducer for Cardiac Color Flow App.DPT · Traditional 05/11/1988SE
K874363Acuson S228 and S328 Transducers for Abdom. Appli.IYO · Traditional 05/02/1988SE
K874922Acuson Transperineal Needle GuideITX · Traditional 02/19/1988SE
K874860Acuson I7505 Transducer for Intracavitary Applica.ITX · Traditional 02/17/1988SE
K871506Acuson L538 TransducerJOP · Traditional 09/28/1987SE
K871416Auxiliary Continuous Wave Doppler TransducerJOP · Traditional 09/28/1987SE
K871239Acuson Physiological Control ModuleDPS · Traditional 06/05/1987SE
K864578Acuson TV519 TransducerHGL · Traditional 03/27/1987SE

Questions and answers

When was Acuson S519 Transducer cleared by the FDA?

Acuson S519 Transducer (K861596) received a 510(k) decision of Substantially Equivalent for Some Indications on July 30, 1986, 92 days after the submission was received.

What is the product code of K861596?

The FDA product code is JOP – Transducer, Ultrasonic, a Class II (moderate risk) device regulated under 21 CFR 870.2880.