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FDA 510(k)

SOCK IT! ORAL PAIN GEL

K-Number: K063148 · 2007-01-17

Decision Date2007-01-17
Product CodeOLR
DecisionSubstantially Equivalent

Device Summary

SOCK IT! ORAL PAIN GEL is the device name listed in this FDA 510(k) record. The listed applicant is Merlin Group Dba Mcmerlin Dental Company. It received FDA 510(k) clearance on 2007-01-17 under 510(k) number K063148. The device is classified under product code OLR. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOCK IT! ORAL PAIN GEL?

SOCK IT! ORAL PAIN GEL is a medical device that received FDA 510(k) clearance on 2007-01-17. The listed applicant is Merlin Group Dba Mcmerlin Dental Company. The 510(k) number is K063148.

When did SOCK IT! ORAL PAIN GEL receive FDA 510(k) clearance?

SOCK IT! ORAL PAIN GEL received FDA 510(k) clearance on 2007-01-17, under 510(k) number K063148.

Who is the listed applicant for SOCK IT! ORAL PAIN GEL?

The FDA 510(k) record lists Merlin Group Dba Mcmerlin Dental Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOCK IT! ORAL PAIN GEL?

The FDA product code for SOCK IT! ORAL PAIN GEL is OLR.

Related Devices (Code: OLR)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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