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FDA 510(k)

HYDROXYLAPATITE ALVEOLAR RIDGE MAIN

K-Number: K810382 · 1981-03-20

ApplicantCarbomedics, Inc.
Decision Date1981-03-20
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HYDROXYLAPATITE ALVEOLAR RIDGE MAIN is the device name listed in this FDA 510(k) record. The listed applicant is Carbomedics, Inc.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K810382. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDROXYLAPATITE ALVEOLAR RIDGE MAIN?

HYDROXYLAPATITE ALVEOLAR RIDGE MAIN is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Carbomedics, Inc.. The 510(k) number is K810382.

When did HYDROXYLAPATITE ALVEOLAR RIDGE MAIN receive FDA 510(k) clearance?

HYDROXYLAPATITE ALVEOLAR RIDGE MAIN received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810382.

Who is the listed applicant for HYDROXYLAPATITE ALVEOLAR RIDGE MAIN?

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

What is the FDA product code for HYDROXYLAPATITE ALVEOLAR RIDGE MAIN?

The FDA product code for HYDROXYLAPATITE ALVEOLAR RIDGE MAIN is LYC.

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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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