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FDA 510(k)

XERORADIOGRAPHY 125 SYSTEM - MODIFIED

K-Number: K761022 · 1976-11-24

Decision Date1976-11-24
Product CodeIXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XERORADIOGRAPHY 125 SYSTEM - MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Xeroradiography. It received FDA 510(k) clearance on 1976-11-24 under 510(k) number K761022. The device is classified under product code IXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XERORADIOGRAPHY 125 SYSTEM - MODIFIED?

XERORADIOGRAPHY 125 SYSTEM - MODIFIED is a medical device that received FDA 510(k) clearance on 1976-11-24. The listed applicant is Xeroradiography. The 510(k) number is K761022.

When did XERORADIOGRAPHY 125 SYSTEM - MODIFIED receive FDA 510(k) clearance?

XERORADIOGRAPHY 125 SYSTEM - MODIFIED received FDA 510(k) clearance on 1976-11-24, under 510(k) number K761022.

Who is the listed applicant for XERORADIOGRAPHY 125 SYSTEM - MODIFIED?

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

What is the FDA product code for XERORADIOGRAPHY 125 SYSTEM - MODIFIED?

The FDA product code for XERORADIOGRAPHY 125 SYSTEM - MODIFIED is IXK.

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.

Related Devices (Code: IXK)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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