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FDA 510(k)

SYSTEM PLUS

K-Number: K073475 · 2008-03-10

Decision Date2008-03-10
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SYSTEM PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Continental Dental Laboratory. It received FDA 510(k) clearance on 2008-03-10 under 510(k) number K073475. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYSTEM PLUS?

SYSTEM PLUS is a medical device that received FDA 510(k) clearance on 2008-03-10. The listed applicant is Continental Dental Laboratory. The 510(k) number is K073475.

When did SYSTEM PLUS receive FDA 510(k) clearance?

SYSTEM PLUS received FDA 510(k) clearance on 2008-03-10, under 510(k) number K073475.

Who is the listed applicant for SYSTEM PLUS?

The FDA 510(k) record lists Continental Dental Laboratory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYSTEM PLUS?

The FDA product code for SYSTEM PLUS is ELW.

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.

Related Devices (Code: ELW)

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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