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FDA 510(k)

TULSA CONTRA ANGLES

K-Number: K012720 · 2001-11-08

ApplicantDentsply Intl.
Decision Date2001-11-08
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TULSA CONTRA ANGLES is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 2001-11-08 under 510(k) number K012720. 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 TULSA CONTRA ANGLES?

TULSA CONTRA ANGLES is a medical device that received FDA 510(k) clearance on 2001-11-08. The listed applicant is Dentsply Intl.. The 510(k) number is K012720.

When did TULSA CONTRA ANGLES receive FDA 510(k) clearance?

TULSA CONTRA ANGLES received FDA 510(k) clearance on 2001-11-08, under 510(k) number K012720.

Who is the listed applicant for TULSA CONTRA ANGLES?

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 TULSA CONTRA ANGLES?

The FDA product code for TULSA CONTRA ANGLES 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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