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FDA 510(k)

NRC NON-RINSE CONDITIONER

K-Number: K992519 · 1999-10-22

ApplicantDentsply Intl.
Decision Date1999-10-22
Product CodeEBC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NRC NON-RINSE CONDITIONER is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1999-10-22 under 510(k) number K992519. The device is classified under product code EBC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NRC NON-RINSE CONDITIONER?

NRC NON-RINSE CONDITIONER is a medical device that received FDA 510(k) clearance on 1999-10-22. The listed applicant is Dentsply Intl.. The 510(k) number is K992519.

When did NRC NON-RINSE CONDITIONER receive FDA 510(k) clearance?

NRC NON-RINSE CONDITIONER received FDA 510(k) clearance on 1999-10-22, under 510(k) number K992519.

Who is the listed applicant for NRC NON-RINSE CONDITIONER?

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 NRC NON-RINSE CONDITIONER?

The FDA product code for NRC NON-RINSE CONDITIONER is EBC.

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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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