FOCISCAN ECHOVISOR SYSTEM

FDA 510(k) Premarket Notification · Submission K781348 · Applicant: Metrix Teknika, Inc.

Public Record 510(k) Submission Decision Date: 1978-10-03 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K781348.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K781348

Applicant / Sponsor

Metrix Teknika, Inc.

Device Name

FOCISCAN ECHOVISOR SYSTEM

Product Code

N/A

Decision Date

1978-10-03

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Unknown ()

Clearance Type

Traditional

Third Party Flag

Date Received

1978-08-07

Public Record Disclaimer

This page represents an index of public-record FDA premarket notification filings. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Information may be outdated or incomplete. Refer to official government source files for critical decisions.