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FDA 510(k)

DIAGNOSTIC ULTRASONIC TRANSDUCER

K-Number: K941593 · 1996-05-17

ApplicantToshiba America Medical Systems, In.C
Decision Date1996-05-17
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTIC ULTRASONIC TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 1996-05-17 under 510(k) number K941593. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAGNOSTIC ULTRASONIC TRANSDUCER?

DIAGNOSTIC ULTRASONIC TRANSDUCER is a medical device that received FDA 510(k) clearance on 1996-05-17. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K941593.

When did DIAGNOSTIC ULTRASONIC TRANSDUCER receive FDA 510(k) clearance?

DIAGNOSTIC ULTRASONIC TRANSDUCER received FDA 510(k) clearance on 1996-05-17, under 510(k) number K941593.

Who is the listed applicant for DIAGNOSTIC ULTRASONIC TRANSDUCER?

The FDA 510(k) record lists Toshiba America Medical Systems, In.C as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAGNOSTIC ULTRASONIC TRANSDUCER?

The FDA product code for DIAGNOSTIC ULTRASONIC TRANSDUCER is IYO.

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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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