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FDA 510(k)

XEROX 128 CASSETTE CHANGER

K-Number: K812024 · 1981-08-13

ApplicantXerox Medical Systems
Decision Date1981-08-13
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XEROX 128 CASSETTE CHANGER 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 1981-08-13 under 510(k) number K812024. The device is classified under product code KPX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XEROX 128 CASSETTE CHANGER?

XEROX 128 CASSETTE CHANGER is a medical device that received FDA 510(k) clearance on 1981-08-13. The listed applicant is Xerox Medical Systems. The 510(k) number is K812024.

When did XEROX 128 CASSETTE CHANGER receive FDA 510(k) clearance?

XEROX 128 CASSETTE CHANGER received FDA 510(k) clearance on 1981-08-13, under 510(k) number K812024.

Who is the listed applicant for XEROX 128 CASSETTE CHANGER?

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 128 CASSETTE CHANGER?

The FDA product code for XEROX 128 CASSETTE CHANGER is KPX.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 SYSTEMK832733XEROX 120 SYS MAMMOGRAPHIC X-RAYK791014DENTAL XERORADIOGRAPHY

Related Devices (Code: KPX)

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.

K945635TRANS X-1000Canon USA, Inc.K935157ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBESRegulatory Consultants TO the Medical Device IndusK934850NUCLEAR ASSOCIATES PERSONNEL PROTECTIVE SHIELDSVictoreen, Inc.K933035BCM-600TXB C Medical , Ltd.K925598BUCKYMATIC AUTOMATIC CHEST FILM CHANGERAcoma Medical Imaging, Inc.K924423MWX-7440 HIGH SPEED BUCKYMidwest X-Ray Equipment Co.

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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