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FDA 510(k)

X-RAY GENERATOR MODEL KXO-15

K-Number: K771294 · 1977-08-03

Decision Date1977-08-03
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY GENERATOR MODEL KXO-15 is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems. It received FDA 510(k) clearance on 1977-08-03 under 510(k) number K771294. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY GENERATOR MODEL KXO-15?

X-RAY GENERATOR MODEL KXO-15 is a medical device that received FDA 510(k) clearance on 1977-08-03. The listed applicant is Toshiba Medical Systems. The 510(k) number is K771294.

When did X-RAY GENERATOR MODEL KXO-15 receive FDA 510(k) clearance?

X-RAY GENERATOR MODEL KXO-15 received FDA 510(k) clearance on 1977-08-03, under 510(k) number K771294.

Who is the listed applicant for X-RAY GENERATOR MODEL KXO-15?

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

What is the FDA product code for X-RAY GENERATOR MODEL KXO-15?

The FDA product code for X-RAY GENERATOR MODEL KXO-15 is IZO.

Related Clinical Trials

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.

Other records listing Toshiba Medical Systems 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.

View all 54 devices →

Related Devices (Code: IZO)

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.

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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