FDA 510(k)

NOVO CEREBROGRAPH

K-Number: K837322 · 1983-04-21

Decision Date1983-04-21

Product Code

DecisionSubstantially Equivalent

Device Summary

NOVO CEREBROGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Novo Diagnostic Systems. It received FDA 510(k) clearance on 1983-04-21 under 510(k) number K837322. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVO CEREBROGRAPH?

NOVO CEREBROGRAPH is a medical device that received FDA 510(k) clearance on 1983-04-21. The listed applicant is Novo Diagnostic Systems. The 510(k) number is K837322.

When did NOVO CEREBROGRAPH receive FDA 510(k) clearance?

NOVO CEREBROGRAPH received FDA 510(k) clearance on 1983-04-21, under 510(k) number K837322.

Who is the listed applicant for NOVO CEREBROGRAPH?

The FDA 510(k) record lists Novo Diagnostic Systems 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 Novo Diagnostic Systems as applicant

K828574NOVO BMC LAB 22A BONE MINERAL CONTENT DETERMINATION IN THE AXIAL SKELETON

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.