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FDA 510(k)

ACUSON V714 TRANSDUCER

K-Number: K920882 · 1993-03-26

ApplicantAcuson Corp.
Decision Date1993-03-26
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACUSON V714 TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Acuson Corp.. It received FDA 510(k) clearance on 1993-03-26 under 510(k) number K920882. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUSON V714 TRANSDUCER?

ACUSON V714 TRANSDUCER is a medical device that received FDA 510(k) clearance on 1993-03-26. The listed applicant is Acuson Corp.. The 510(k) number is K920882.

When did ACUSON V714 TRANSDUCER receive FDA 510(k) clearance?

ACUSON V714 TRANSDUCER received FDA 510(k) clearance on 1993-03-26, under 510(k) number K920882.

Who is the listed applicant for ACUSON V714 TRANSDUCER?

The FDA 510(k) record lists Acuson Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACUSON V714 TRANSDUCER?

The FDA product code for ACUSON V714 TRANSDUCER is ITX.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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