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FDA 510(k)

LAIMAD

K-Number: K062333 · 2006-12-14

ApplicantSteven Lamberg, D.D.S
Decision Date2006-12-14
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LAIMAD is the device name listed in this FDA 510(k) record. The listed applicant is Steven Lamberg, D.D.S. It received FDA 510(k) clearance on 2006-12-14 under 510(k) number K062333. 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 LAIMAD?

LAIMAD is a medical device that received FDA 510(k) clearance on 2006-12-14. The listed applicant is Steven Lamberg, D.D.S. The 510(k) number is K062333.

When did LAIMAD receive FDA 510(k) clearance?

LAIMAD received FDA 510(k) clearance on 2006-12-14, under 510(k) number K062333.

Who is the listed applicant for LAIMAD?

The FDA 510(k) record lists Steven Lamberg, D.D.S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAIMAD?

The FDA product code for LAIMAD 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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