CARDIO REVUE CENTER— 510(k) K820820

Substantially Equivalent

Diasonics, Inc.

FDA 510(k) clearance K820820 for CARDIO REVUE CENTER, Substantially Equivalent on 1982-04-29. Applicant: Diasonics, Inc.. Device class: 2.

Clearance details

Applicant: Diasonics, Inc.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1982-03-24
Decision date: 1982-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.