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FDA 510(k)

INTEGRITY

K-Number: K853052 · 1985-08-16

ApplicantDentsply Intl.
Decision Date1985-08-16
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTEGRITY is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1985-08-16 under 510(k) number K853052. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEGRITY?

INTEGRITY is a medical device that received FDA 510(k) clearance on 1985-08-16. The listed applicant is Dentsply Intl.. The 510(k) number is K853052.

When did INTEGRITY receive FDA 510(k) clearance?

INTEGRITY received FDA 510(k) clearance on 1985-08-16, under 510(k) number K853052.

Who is the listed applicant for INTEGRITY?

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 INTEGRITY?

The FDA product code for INTEGRITY is EBG.

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Related Devices (Code: EBG)

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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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