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FDA 510(k)

ACUSON S519B TRANSDUCER

K-Number: K863236 · 1987-02-13

ApplicantAcuson Computed Sonography
Decision Date1987-02-13
Product Code
DecisionSubstantially Equivalent

Device Summary

ACUSON S519B TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Acuson Computed Sonography. It received FDA 510(k) clearance on 1987-02-13 under 510(k) number K863236. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUSON S519B TRANSDUCER?

ACUSON S519B TRANSDUCER is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Acuson Computed Sonography. The 510(k) number is K863236.

When did ACUSON S519B TRANSDUCER receive FDA 510(k) clearance?

ACUSON S519B TRANSDUCER received FDA 510(k) clearance on 1987-02-13, under 510(k) number K863236.

Who is the listed applicant for ACUSON S519B TRANSDUCER?

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

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Other records listing Acuson Computed Sonography as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K893863ACUSON L538 TRANSDUCERK874028ACUSON S328 TRANSDUCERK874861ACUSON S328 TRANSDUCER FOR CARDIAC COLOR FLOW APP.K874363ACUSON S228 AND S328 TRANSDUCERS FOR ABDOM. APPLI.K874922ACUSON TRANSPERINEAL NEEDLE GUIDEK874860ACUSON I7505 TRANSDUCER FOR INTRACAVITARY APPLICA.

View all 24 devices →

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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