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FDA 510(k)

ENDSNOR

K-Number: K072731 · 2008-06-12

ApplicantDockstader Orthodontic Lab, Inc.
Decision Date2008-06-12
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDSNOR is the device name listed in this FDA 510(k) record. The listed applicant is Dockstader Orthodontic Lab, Inc.. It received FDA 510(k) clearance on 2008-06-12 under 510(k) number K072731. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDSNOR?

ENDSNOR is a medical device that received FDA 510(k) clearance on 2008-06-12. The listed applicant is Dockstader Orthodontic Lab, Inc.. The 510(k) number is K072731.

When did ENDSNOR receive FDA 510(k) clearance?

ENDSNOR received FDA 510(k) clearance on 2008-06-12, under 510(k) number K072731.

Who is the listed applicant for ENDSNOR?

The FDA 510(k) record lists Dockstader Orthodontic Lab, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDSNOR?

The FDA product code for ENDSNOR is LRK.

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Related Devices (Code: LRK)

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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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