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FDA 510(k)

VIDEO-DILUTION TECH. MARK I INSTRUMENT

K-Number: K831057 · 1983-10-19

ApplicantAngio Tec Corp.
Decision Date1983-10-19
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VIDEO-DILUTION TECH. MARK I INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Angio Tec Corp.. It received FDA 510(k) clearance on 1983-10-19 under 510(k) number K831057. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDEO-DILUTION TECH. MARK I INSTRUMENT?

VIDEO-DILUTION TECH. MARK I INSTRUMENT is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Angio Tec Corp.. The 510(k) number is K831057.

When did VIDEO-DILUTION TECH. MARK I INSTRUMENT receive FDA 510(k) clearance?

VIDEO-DILUTION TECH. MARK I INSTRUMENT received FDA 510(k) clearance on 1983-10-19, under 510(k) number K831057.

Who is the listed applicant for VIDEO-DILUTION TECH. MARK I INSTRUMENT?

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

What is the FDA product code for VIDEO-DILUTION TECH. MARK I INSTRUMENT?

The FDA product code for VIDEO-DILUTION TECH. MARK I INSTRUMENT is DXG.

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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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