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FDA 510(k)

POLYSTAR 79 DENTURE BASE RESIN

K-Number: K072851 · 2008-02-20

Decision Date2008-02-20
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POLYSTAR 79 DENTURE BASE RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Cmp Industries, LLC. It received FDA 510(k) clearance on 2008-02-20 under 510(k) number K072851. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLYSTAR 79 DENTURE BASE RESIN?

POLYSTAR 79 DENTURE BASE RESIN is a medical device that received FDA 510(k) clearance on 2008-02-20. The listed applicant is Cmp Industries, LLC. The 510(k) number is K072851.

When did POLYSTAR 79 DENTURE BASE RESIN receive FDA 510(k) clearance?

POLYSTAR 79 DENTURE BASE RESIN received FDA 510(k) clearance on 2008-02-20, under 510(k) number K072851.

Who is the listed applicant for POLYSTAR 79 DENTURE BASE RESIN?

The FDA 510(k) record lists Cmp Industries, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POLYSTAR 79 DENTURE BASE RESIN?

The FDA product code for POLYSTAR 79 DENTURE BASE RESIN is EBI.

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 Cmp Industries, LLC 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.

View all 7 devices →

Related Devices (Code: EBI)

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

View on FDA Database →

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

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