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FDA 510(k)

ENDODONTIC POST W/ ACCESSORIES

K-Number: K923232 · 1993-03-05

ApplicantVeillette Ent.
Decision Date1993-03-05
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDODONTIC POST W/ ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Veillette Ent.. It received FDA 510(k) clearance on 1993-03-05 under 510(k) number K923232. The device is classified under product code ELR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDODONTIC POST W/ ACCESSORIES?

ENDODONTIC POST W/ ACCESSORIES is a medical device that received FDA 510(k) clearance on 1993-03-05. The listed applicant is Veillette Ent.. The 510(k) number is K923232.

When did ENDODONTIC POST W/ ACCESSORIES receive FDA 510(k) clearance?

ENDODONTIC POST W/ ACCESSORIES received FDA 510(k) clearance on 1993-03-05, under 510(k) number K923232.

Who is the listed applicant for ENDODONTIC POST W/ ACCESSORIES?

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

What is the FDA product code for ENDODONTIC POST W/ ACCESSORIES?

The FDA product code for ENDODONTIC POST W/ ACCESSORIES is ELR.

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Related Devices (Code: ELR)

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.

K060075FIBER-METAL POSTForemost Dental, LLCK042848FRC POSTEC PLUSIvoclar Vivadent, Inc.K030820EVERSTICK POSTStick Tech , Ltd.K020431FIBIOCOREEst. AnthogyrK012496CARBON POSTJ. Morita USA, Inc.K013802FRC POSTECIvoclar Vivadent, Inc.

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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