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FDA 510(k)

ES/ULTRA DISPLAY AND PROCESSING STATION

K-Number: K905412 · 1991-03-25

ApplicantToshiba America Medical Systems, In.C
Decision Date1991-03-25
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ES/ULTRA DISPLAY AND PROCESSING STATION 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 1991-03-25 under 510(k) number K905412. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ES/ULTRA DISPLAY AND PROCESSING STATION?

ES/ULTRA DISPLAY AND PROCESSING STATION is a medical device that received FDA 510(k) clearance on 1991-03-25. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K905412.

When did ES/ULTRA DISPLAY AND PROCESSING STATION receive FDA 510(k) clearance?

ES/ULTRA DISPLAY AND PROCESSING STATION received FDA 510(k) clearance on 1991-03-25, under 510(k) number K905412.

Who is the listed applicant for ES/ULTRA DISPLAY AND PROCESSING STATION?

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 ES/ULTRA DISPLAY AND PROCESSING STATION?

The FDA product code for ES/ULTRA DISPLAY AND PROCESSING STATION is IYX.

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Related Devices (Code: IYX)

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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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