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FDA 510(k)

TEMPORARY DISCLOSING SOLUTION

K-Number: K874074 · 1987-12-29

ApplicantDentsply Intl.
Decision Date1987-12-29
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TEMPORARY DISCLOSING SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K874074. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPORARY DISCLOSING SOLUTION?

TEMPORARY DISCLOSING SOLUTION is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Dentsply Intl.. The 510(k) number is K874074.

When did TEMPORARY DISCLOSING SOLUTION receive FDA 510(k) clearance?

TEMPORARY DISCLOSING SOLUTION received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874074.

Who is the listed applicant for TEMPORARY DISCLOSING SOLUTION?

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 TEMPORARY DISCLOSING SOLUTION?

The FDA product code for TEMPORARY DISCLOSING SOLUTION is KLE.

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Related Devices (Code: KLE)

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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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