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FDA 510(k)

XEROX 120 SYS MAMMOGRAPHIC X-RAY

K-Number: K832733 · 1983-09-29

ApplicantXerox Medical Systems
Decision Date1983-09-29
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XEROX 120 SYS MAMMOGRAPHIC X-RAY is the device name listed in this FDA 510(k) record. The listed applicant is Xerox Medical Systems. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K832733. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XEROX 120 SYS MAMMOGRAPHIC X-RAY?

XEROX 120 SYS MAMMOGRAPHIC X-RAY is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Xerox Medical Systems. The 510(k) number is K832733.

When did XEROX 120 SYS MAMMOGRAPHIC X-RAY receive FDA 510(k) clearance?

XEROX 120 SYS MAMMOGRAPHIC X-RAY received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832733.

Who is the listed applicant for XEROX 120 SYS MAMMOGRAPHIC X-RAY?

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

What is the FDA product code for XEROX 120 SYS MAMMOGRAPHIC X-RAY?

The FDA product code for XEROX 120 SYS MAMMOGRAPHIC X-RAY is IZH.

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Other records listing Xerox 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.

K853459XERORADIOGRAPHY LIQUID TONER IMAGING SYSTEMK833243MAMMOGRAPHIC S-RAY SYSTEMK812024XEROX 128 CASSETTE CHANGERK791014DENTAL XERORADIOGRAPHY

Related Devices (Code: IZH)

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.

K203509SMART FINDERIms Giotto S.P.A.K202294Affirm Contrast BiopsyHologic, Inc.K191495Biopsy PositionerFujifilm CorporationK161575Affirm Lateral Arm Upright Biopsy AccessoryHologicK161920Comfort CoverPrecision Dynamics CorporationK153486Affirm Prone Biopsy SystemHologic, Inc.

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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