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FDA 510(k)

PLAQUE-SWEEP

K-Number: K873209 · 1987-08-25

ApplicantDentsply Intl.
Decision Date1987-08-25
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PLAQUE-SWEEP is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1987-08-25 under 510(k) number K873209. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLAQUE-SWEEP?

PLAQUE-SWEEP is a medical device that received FDA 510(k) clearance on 1987-08-25. The listed applicant is Dentsply Intl.. The 510(k) number is K873209.

When did PLAQUE-SWEEP receive FDA 510(k) clearance?

PLAQUE-SWEEP received FDA 510(k) clearance on 1987-08-25, under 510(k) number K873209.

Who is the listed applicant for PLAQUE-SWEEP?

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 PLAQUE-SWEEP?

The FDA product code for PLAQUE-SWEEP is EFB.

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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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