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FDA 510(k)

COMPOSITE RESIN CORE PASTE MATERIAL

K-Number: K921174 · 1992-09-01

ApplicantCentrix, Inc.
Decision Date1992-09-01
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COMPOSITE RESIN CORE PASTE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 1992-09-01 under 510(k) number K921174. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPOSITE RESIN CORE PASTE MATERIAL?

COMPOSITE RESIN CORE PASTE MATERIAL is a medical device that received FDA 510(k) clearance on 1992-09-01. The listed applicant is Centrix, Inc.. The 510(k) number is K921174.

When did COMPOSITE RESIN CORE PASTE MATERIAL receive FDA 510(k) clearance?

COMPOSITE RESIN CORE PASTE MATERIAL received FDA 510(k) clearance on 1992-09-01, under 510(k) number K921174.

Who is the listed applicant for COMPOSITE RESIN CORE PASTE MATERIAL?

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

What is the FDA product code for COMPOSITE RESIN CORE PASTE MATERIAL?

The FDA product code for COMPOSITE RESIN CORE PASTE MATERIAL is EBF.

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 Centrix, Inc. 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 46 devices →

Related Devices (Code: EBF)

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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