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FDA 510(k)

F-100 FLUOROSCOPIC CONTROL AND XF-100 HIGH VOLTAGE GENERATOR

K-Number: K828575 · 1983-01-03

ApplicantInterchange Manufacturer Corp.
Decision Date1983-01-03
Product Code
DecisionSubstantially Equivalent

Device Summary

F-100 FLUOROSCOPIC CONTROL AND XF-100 HIGH VOLTAGE GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Interchange Manufacturer Corp.. It received FDA 510(k) clearance on 1983-01-03 under 510(k) number K828575. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the F-100 FLUOROSCOPIC CONTROL AND XF-100 HIGH VOLTAGE GENERATOR?

F-100 FLUOROSCOPIC CONTROL AND XF-100 HIGH VOLTAGE GENERATOR is a medical device that received FDA 510(k) clearance on 1983-01-03. The listed applicant is Interchange Manufacturer Corp.. The 510(k) number is K828575.

When did F-100 FLUOROSCOPIC CONTROL AND XF-100 HIGH VOLTAGE GENERATOR receive FDA 510(k) clearance?

F-100 FLUOROSCOPIC CONTROL AND XF-100 HIGH VOLTAGE GENERATOR received FDA 510(k) clearance on 1983-01-03, under 510(k) number K828575.

Who is the listed applicant for F-100 FLUOROSCOPIC CONTROL AND XF-100 HIGH VOLTAGE GENERATOR?

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

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.

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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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