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FDA 510(k)

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

K-Number: K828574 · 1983-04-04

Decision Date1983-04-04
Product Code
DecisionSubstantially Equivalent

Device Summary

NOVO BMC LAB 22A BONE MINERAL CONTENT DETERMINATION IN THE AXIAL SKELETON 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 1983-04-04 under 510(k) number K828574. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVO BMC LAB 22A BONE MINERAL CONTENT DETERMINATION IN THE AXIAL SKELETON?

NOVO BMC LAB 22A BONE MINERAL CONTENT DETERMINATION IN THE AXIAL SKELETON is a medical device that received FDA 510(k) clearance on 1983-04-04. The listed applicant is Novo Diagnostic Systems. The 510(k) number is K828574.

When did NOVO BMC LAB 22A BONE MINERAL CONTENT DETERMINATION IN THE AXIAL SKELETON receive FDA 510(k) clearance?

NOVO BMC LAB 22A BONE MINERAL CONTENT DETERMINATION IN THE AXIAL SKELETON received FDA 510(k) clearance on 1983-04-04, under 510(k) number K828574.

Who is the listed applicant for NOVO BMC LAB 22A BONE MINERAL CONTENT DETERMINATION IN THE AXIAL SKELETON?

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.

Other records listing Novo Diagnostic Systems as applicant

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.

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.

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