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FDA 510(k)

DENTAL LINK

K-Number: K930527 · 1993-06-21

ApplicantEscan, Inc.
Decision Date1993-06-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DENTAL LINK is the device name listed in this FDA 510(k) record. The listed applicant is Escan, Inc.. It received FDA 510(k) clearance on 1993-06-21 under 510(k) number K930527. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL LINK?

DENTAL LINK is a medical device that received FDA 510(k) clearance on 1993-06-21. The listed applicant is Escan, Inc.. The 510(k) number is K930527.

When did DENTAL LINK receive FDA 510(k) clearance?

DENTAL LINK received FDA 510(k) clearance on 1993-06-21, under 510(k) number K930527.

Who is the listed applicant for DENTAL LINK?

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

What is the FDA product code for DENTAL LINK?

The FDA product code for DENTAL LINK is LLZ.

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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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