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FDA 510(k)

FRIADENT ESTHETICAP

K-Number: K050208 · 2005-06-14

ApplicantDentsply International
Decision Date2005-06-14
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FRIADENT ESTHETICAP is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply International. It received FDA 510(k) clearance on 2005-06-14 under 510(k) number K050208. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRIADENT ESTHETICAP?

FRIADENT ESTHETICAP is a medical device that received FDA 510(k) clearance on 2005-06-14. The listed applicant is Dentsply International. The 510(k) number is K050208.

When did FRIADENT ESTHETICAP receive FDA 510(k) clearance?

FRIADENT ESTHETICAP received FDA 510(k) clearance on 2005-06-14, under 510(k) number K050208.

Who is the listed applicant for FRIADENT ESTHETICAP?

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

What is the FDA product code for FRIADENT ESTHETICAP?

The FDA product code for FRIADENT ESTHETICAP is NHA.

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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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