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FDA 510(k)

MODEL 1812 CONTROL CONSOLE, ACCESSORIEX

K-Number: K780952 · 1978-08-31

ApplicantMedtronic Vascular
Decision Date1978-08-31
Product CodeDWA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 1812 CONTROL CONSOLE, ACCESSORIEX is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1978-08-31 under 510(k) number K780952. The device is classified under product code DWA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 1812 CONTROL CONSOLE, ACCESSORIEX?

MODEL 1812 CONTROL CONSOLE, ACCESSORIEX is a medical device that received FDA 510(k) clearance on 1978-08-31. The listed applicant is Medtronic Vascular. The 510(k) number is K780952.

When did MODEL 1812 CONTROL CONSOLE, ACCESSORIEX receive FDA 510(k) clearance?

MODEL 1812 CONTROL CONSOLE, ACCESSORIEX received FDA 510(k) clearance on 1978-08-31, under 510(k) number K780952.

Who is the listed applicant for MODEL 1812 CONTROL CONSOLE, ACCESSORIEX?

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

What is the FDA product code for MODEL 1812 CONTROL CONSOLE, ACCESSORIEX?

The FDA product code for MODEL 1812 CONTROL CONSOLE, ACCESSORIEX is DWA.

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Related Devices (Code: DWA)

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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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