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FDA 510(k)

THE SUAD DEVICE

K-Number: K023836 · 2003-07-08

ApplicantStrong Dental, Inc.
Decision Date2003-07-08
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE SUAD DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Strong Dental, Inc.. It received FDA 510(k) clearance on 2003-07-08 under 510(k) number K023836. 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 THE SUAD DEVICE?

THE SUAD DEVICE is a medical device that received FDA 510(k) clearance on 2003-07-08. The listed applicant is Strong Dental, Inc.. The 510(k) number is K023836.

When did THE SUAD DEVICE receive FDA 510(k) clearance?

THE SUAD DEVICE received FDA 510(k) clearance on 2003-07-08, under 510(k) number K023836.

Who is the listed applicant for THE SUAD DEVICE?

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

What is the FDA product code for THE SUAD DEVICE?

The FDA product code for THE SUAD DEVICE is LRK.

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Related Devices (Code: LRK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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