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FDA 510(k)

ACUSON C366 TRANSDUCER

K-Number: K911916 · 1992-06-18

ApplicantAcuson Corp.
Decision Date1992-06-18
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACUSON C366 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 1992-06-18 under 510(k) number K911916. 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 C366 TRANSDUCER?

ACUSON C366 TRANSDUCER is a medical device that received FDA 510(k) clearance on 1992-06-18. The listed applicant is Acuson Corp.. The 510(k) number is K911916.

When did ACUSON C366 TRANSDUCER receive FDA 510(k) clearance?

ACUSON C366 TRANSDUCER received FDA 510(k) clearance on 1992-06-18, under 510(k) number K911916.

Who is the listed applicant for ACUSON C366 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 C366 TRANSDUCER?

The FDA product code for ACUSON C366 TRANSDUCER is ITX.

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Other records listing Acuson Corp. as applicant

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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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