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FDA 510(k)

MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C

K-Number: K850761 · 1985-09-19

Decision Date1985-09-19
Product CodeBZN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C is the device name listed in this FDA 510(k) record. The listed applicant is Medicor USA , Ltd.. It received FDA 510(k) clearance on 1985-09-19 under 510(k) number K850761. The device is classified under product code BZN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C?

MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C is a medical device that received FDA 510(k) clearance on 1985-09-19. The listed applicant is Medicor USA , Ltd.. The 510(k) number is K850761.

When did MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C receive FDA 510(k) clearance?

MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C received FDA 510(k) clearance on 1985-09-19, under 510(k) number K850761.

Who is the listed applicant for MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C?

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

What is the FDA product code for MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C?

The FDA product code for MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY C is BZN.

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 Medicor USA , Ltd. 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 14 devices →

Related Devices (Code: BZN)

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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