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FDA 510(k)

MODIFICATION OF ACUSON V510B TRANSDUCER

K-Number: K933663 · 1994-01-21

ApplicantAcuson Corp.
Decision Date1994-01-21
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF ACUSON V510B 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 1994-01-21 under 510(k) number K933663. 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 MODIFICATION OF ACUSON V510B TRANSDUCER?

MODIFICATION OF ACUSON V510B TRANSDUCER is a medical device that received FDA 510(k) clearance on 1994-01-21. The listed applicant is Acuson Corp.. The 510(k) number is K933663.

When did MODIFICATION OF ACUSON V510B TRANSDUCER receive FDA 510(k) clearance?

MODIFICATION OF ACUSON V510B TRANSDUCER received FDA 510(k) clearance on 1994-01-21, under 510(k) number K933663.

Who is the listed applicant for MODIFICATION OF ACUSON V510B 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 MODIFICATION OF ACUSON V510B TRANSDUCER?

The FDA product code for MODIFICATION OF ACUSON V510B 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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