FDA 510(k)

FOCISCAN ECHOVISOR SYSTEM

K-Number: K781348 · 1978-10-03

Decision Date1978-10-03

Product Code

DecisionSubstantially Equivalent

Device Summary

FOCISCAN ECHOVISOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Metrix Teknika, Inc.. It received FDA 510(k) clearance on 1978-10-03 under 510(k) number K781348. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOCISCAN ECHOVISOR SYSTEM?

FOCISCAN ECHOVISOR SYSTEM is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is Metrix Teknika, Inc.. The 510(k) number is K781348.

When did FOCISCAN ECHOVISOR SYSTEM receive FDA 510(k) clearance?

FOCISCAN ECHOVISOR SYSTEM received FDA 510(k) clearance on 1978-10-03, under 510(k) number K781348.

Who is the listed applicant for FOCISCAN ECHOVISOR SYSTEM?

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

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Metrix Teknika, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.