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FDA 510(k)

BETA POST

K-Number: K812092 · 1981-08-20

ApplicantPaul B. Heller, D.M.D.
Decision Date1981-08-20
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BETA POST is the device name listed in this FDA 510(k) record. The listed applicant is Paul B. Heller, D.M.D.. It received FDA 510(k) clearance on 1981-08-20 under 510(k) number K812092. 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 BETA POST?

BETA POST is a medical device that received FDA 510(k) clearance on 1981-08-20. The listed applicant is Paul B. Heller, D.M.D.. The 510(k) number is K812092.

When did BETA POST receive FDA 510(k) clearance?

BETA POST received FDA 510(k) clearance on 1981-08-20, under 510(k) number K812092.

Who is the listed applicant for BETA POST?

The FDA 510(k) record lists Paul B. Heller, D.M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BETA POST?

The FDA product code for BETA POST is ELR.

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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