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FDA 510(k)

ROOT CANAL POST

K-Number: K924376 · 1993-11-22

ApplicantThe Thera Group
Decision Date1993-11-22
Product CodeEBL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ROOT CANAL POST is the device name listed in this FDA 510(k) record. The listed applicant is The Thera Group. It received FDA 510(k) clearance on 1993-11-22 under 510(k) number K924376. The device is classified under product code EBL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROOT CANAL POST?

ROOT CANAL POST is a medical device that received FDA 510(k) clearance on 1993-11-22. The listed applicant is The Thera Group. The 510(k) number is K924376.

When did ROOT CANAL POST receive FDA 510(k) clearance?

ROOT CANAL POST received FDA 510(k) clearance on 1993-11-22, under 510(k) number K924376.

Who is the listed applicant for ROOT CANAL POST?

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

What is the FDA product code for ROOT CANAL POST?

The FDA product code for ROOT CANAL POST is EBL.

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Related Devices (Code: EBL)

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.

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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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