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FDA 510(k)

INTEGRAPOST

K-Number: K942528 · 1994-08-05

ApplicantDental Logics, Inc.
Decision Date1994-08-05
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTEGRAPOST is the device name listed in this FDA 510(k) record. The listed applicant is Dental Logics, Inc.. It received FDA 510(k) clearance on 1994-08-05 under 510(k) number K942528. 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 INTEGRAPOST?

INTEGRAPOST is a medical device that received FDA 510(k) clearance on 1994-08-05. The listed applicant is Dental Logics, Inc.. The 510(k) number is K942528.

When did INTEGRAPOST receive FDA 510(k) clearance?

INTEGRAPOST received FDA 510(k) clearance on 1994-08-05, under 510(k) number K942528.

Who is the listed applicant for INTEGRAPOST?

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

What is the FDA product code for INTEGRAPOST?

The FDA product code for INTEGRAPOST 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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