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FDA 510(k)

ARCEE DENTAL POST

K-Number: K851038 · 1985-04-29

Decision Date1985-04-29
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ARCEE DENTAL POST is the device name listed in this FDA 510(k) record. The listed applicant is Arcee Dental Products Co.. It received FDA 510(k) clearance on 1985-04-29 under 510(k) number K851038. 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 ARCEE DENTAL POST?

ARCEE DENTAL POST is a medical device that received FDA 510(k) clearance on 1985-04-29. The listed applicant is Arcee Dental Products Co.. The 510(k) number is K851038.

When did ARCEE DENTAL POST receive FDA 510(k) clearance?

ARCEE DENTAL POST received FDA 510(k) clearance on 1985-04-29, under 510(k) number K851038.

Who is the listed applicant for ARCEE DENTAL POST?

The FDA 510(k) record lists Arcee Dental Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARCEE DENTAL POST?

The FDA product code for ARCEE DENTAL POST is ELR.

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.

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.

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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