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FDA 510(k)

ABRASIVE WHEELS

K-Number: K781777 · 1978-12-20

ApplicantDentsply Intl.
Decision Date1978-12-20
Product CodeEJQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ABRASIVE WHEELS is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1978-12-20 under 510(k) number K781777. The device is classified under product code EJQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABRASIVE WHEELS?

ABRASIVE WHEELS is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Dentsply Intl.. The 510(k) number is K781777.

When did ABRASIVE WHEELS receive FDA 510(k) clearance?

ABRASIVE WHEELS received FDA 510(k) clearance on 1978-12-20, under 510(k) number K781777.

Who is the listed applicant for ABRASIVE WHEELS?

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 ABRASIVE WHEELS?

The FDA product code for ABRASIVE WHEELS is EJQ.

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Other records listing Dentsply Intl. as applicant

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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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