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FDA 510(k)

MINI MASSEUSE

K-Number: K110057 · 2011-10-28

ApplicantMj Specialty Retail
Decision Date2011-10-28
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MINI MASSEUSE is the device name listed in this FDA 510(k) record. The listed applicant is Mj Specialty Retail. It received FDA 510(k) clearance on 2011-10-28 under 510(k) number K110057. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI MASSEUSE?

MINI MASSEUSE is a medical device that received FDA 510(k) clearance on 2011-10-28. The listed applicant is Mj Specialty Retail. The 510(k) number is K110057.

When did MINI MASSEUSE receive FDA 510(k) clearance?

MINI MASSEUSE received FDA 510(k) clearance on 2011-10-28, under 510(k) number K110057.

Who is the listed applicant for MINI MASSEUSE?

The FDA 510(k) record lists Mj Specialty Retail as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI MASSEUSE?

The FDA product code for MINI MASSEUSE is NGX.

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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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