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FDA 510(k)

THE MODEL 3003 SCALER

K-Number: K930698 · 1993-07-22

ApplicantDentsply Intl.
Decision Date1993-07-22
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE MODEL 3003 SCALER is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K930698. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE MODEL 3003 SCALER?

THE MODEL 3003 SCALER is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Dentsply Intl.. The 510(k) number is K930698.

When did THE MODEL 3003 SCALER receive FDA 510(k) clearance?

THE MODEL 3003 SCALER received FDA 510(k) clearance on 1993-07-22, under 510(k) number K930698.

Who is the listed applicant for THE MODEL 3003 SCALER?

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 THE MODEL 3003 SCALER?

The FDA product code for THE MODEL 3003 SCALER is ELC.

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Related Devices (Code: ELC)

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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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