K781348Substantially Equivalent

Fociscan Echovisor System

Name: K781348 Fociscan Echovisor System
Creator: Metrix Teknika, Inc.
Published: 1978-10-03
License: https://open.fda.gov/license/

Metrix Teknika, Inc., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K781348 is the FDA 510(k) clearance record for FOCISCAN ECHOVISOR SYSTEM, cleared for Metrix Teknika, Inc. on 1978-10-03. FDA records list 4 510(k) clearances for Metrix Teknika, Inc., from 1978-03-06 to 1979-01-17. As of 2026-09-10, FDA records show no recalls naming K781348.

Clearance record

Decision date: 1978-10-03
Received: 1978-08-07 (57 days to decision)
Review panel: Unknown
Applicant: Metrix Teknika, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No