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FDA 510(k)

PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL

K-Number: K022675 · 2002-11-07

Decision Date2002-11-07
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Prime Dental Manufacturing, Inc.. It received FDA 510(k) clearance on 2002-11-07 under 510(k) number K022675. 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 PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL?

PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL is a medical device that received FDA 510(k) clearance on 2002-11-07. The listed applicant is Prime Dental Manufacturing, Inc.. The 510(k) number is K022675.

When did PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL receive FDA 510(k) clearance?

PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL received FDA 510(k) clearance on 2002-11-07, under 510(k) number K022675.

Who is the listed applicant for PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL?

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

What is the FDA product code for PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL?

The FDA product code for PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP 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 Prime Dental Manufacturing, 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 9 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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