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FDA 510(k)

CARDIO REVUE CENTER

K-Number: K820820 · 1982-04-29

ApplicantDiasonics, Inc.
Decision Date1982-04-29
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIO REVUE CENTER is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1982-04-29 under 510(k) number K820820. 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 CARDIO REVUE CENTER?

CARDIO REVUE CENTER is a medical device that received FDA 510(k) clearance on 1982-04-29. The listed applicant is Diasonics, Inc.. The 510(k) number is K820820.

When did CARDIO REVUE CENTER receive FDA 510(k) clearance?

CARDIO REVUE CENTER received FDA 510(k) clearance on 1982-04-29, under 510(k) number K820820.

Who is the listed applicant for CARDIO REVUE CENTER?

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

What is the FDA product code for CARDIO REVUE CENTER?

The FDA product code for CARDIO REVUE CENTER is DXG.

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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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