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FDA 510(k)

CARRARA PRESS SYSTEM

K-Number: K033667 · 2004-01-23

ApplicantDentsply Intl.
Decision Date2004-01-23
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CARRARA PRESS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 2004-01-23 under 510(k) number K033667. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARRARA PRESS SYSTEM?

CARRARA PRESS SYSTEM is a medical device that received FDA 510(k) clearance on 2004-01-23. The listed applicant is Dentsply Intl.. The 510(k) number is K033667.

When did CARRARA PRESS SYSTEM receive FDA 510(k) clearance?

CARRARA PRESS SYSTEM received FDA 510(k) clearance on 2004-01-23, under 510(k) number K033667.

Who is the listed applicant for CARRARA PRESS SYSTEM?

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

What is the FDA product code for CARRARA PRESS SYSTEM?

The FDA product code for CARRARA PRESS SYSTEM is EIH.

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Related Devices (Code: EIH)

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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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