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FDA 510(k)

GOOD NIGHT

K-Number: K102463 · 2011-05-25

ApplicantLarry V Connell, Dmd
Decision Date2011-05-25
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GOOD NIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Larry V Connell, Dmd. It received FDA 510(k) clearance on 2011-05-25 under 510(k) number K102463. 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 GOOD NIGHT?

GOOD NIGHT is a medical device that received FDA 510(k) clearance on 2011-05-25. The listed applicant is Larry V Connell, Dmd. The 510(k) number is K102463.

When did GOOD NIGHT receive FDA 510(k) clearance?

GOOD NIGHT received FDA 510(k) clearance on 2011-05-25, under 510(k) number K102463.

Who is the listed applicant for GOOD NIGHT?

The FDA 510(k) record lists Larry V Connell, Dmd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GOOD NIGHT?

The FDA product code for GOOD NIGHT 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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