Acuson V328 and C5432 Transducers

FDA 510(k) K897151 · Acuson Corp.

Substantially Equivalent

510(k) numberK897151

Submission

Device name
Acuson V328 and C5432 Transducers
Applicant
Acuson Corp.
Mountain View, CA, US
Received
December 26, 1989
Decision date
July 3, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JTX – Transport Systems, Anaerobic
Device class
Class I (low risk)
Regulation
21 CFR 866.2900
Specialty
Microbiology

Other 510(k)s with product code JTX

510(k)DeviceApplicantDecision
K901645Anaerobic Accu-Culshure(Tm)JTX · Traditional Medical Laboratory Automation Systems, Inc.07/16/1990SE
K882637Accu-Culshure TMJTX · Traditional Accu-Med Corp.07/06/1988SE
K791724Bio-Bag Environmental Chamber (a & B)JTX · Traditional Marion Laboratories, Inc.10/17/1979SE
K781376Standardize TGCL & TGCHJTX · Traditional American Monitor Corp.09/14/1978SE
K780159AnaswabJTX · Traditional Scott Laboratories, Inc.02/13/1978SE
K761241Pre-Duced Surgi-Swab & Transporter TubeJTX · Traditional Gibco Laboratories Life Technologies, Inc.12/30/1976SE
K760063Specimen Collector, AnaerobicJTX · Traditional Bd Becton Dickinson Vacutainer Systems Preanalytic08/03/1976SE

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Questions and answers

When was Acuson V328 and C5432 Transducers cleared by the FDA?

Acuson V328 and C5432 Transducers (K897151) received a 510(k) decision of Substantially Equivalent on July 3, 1990, 189 days after the submission was received.

What is the product code of K897151?

The FDA product code is JTX – Transport Systems, Anaerobic, a Class I (low risk) device regulated under 21 CFR 866.2900.