K827573Substantially Equivalent

Diasonics Cardio/imaging Echoscope

Name: K827573 Diasonics Cardio/imaging Echoscope
Creator: Diasonics, Inc.
Published: 1982-08-16
License: https://open.fda.gov/license/

Diasonics, Inc., Milpitas CA / Traditional, Substantially Equivalent

FDA source

K827573 is the FDA 510(k) clearance record for DIASONICS CARDIO/IMAGING ECHOSCOPE, cleared for Diasonics, Inc. on 1982-08-16. FDA records list 42 510(k) clearances for Diasonics, Inc., from 1978-10-10 to 1997-01-02. As of 2026-09-10, FDA records show no recalls naming K827573.

Clearance record

Decision date: 1982-08-16
Received: 1982-07-23 (24 days to decision)
Review panel: Unknown
Applicant: Diasonics, Inc. 1708 Mc Carthy Blvd., Milpitas CA
Third party review: No