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FDA 510(k)

LUMANOSITY CELEBRITY, MODEL 204

K-Number: K100213 · 2010-10-04

ApplicantLumanosity, Inc.
Decision Date2010-10-04
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LUMANOSITY CELEBRITY, MODEL 204 is the device name listed in this FDA 510(k) record. The listed applicant is Lumanosity, Inc.. It received FDA 510(k) clearance on 2010-10-04 under 510(k) number K100213. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUMANOSITY CELEBRITY, MODEL 204?

LUMANOSITY CELEBRITY, MODEL 204 is a medical device that received FDA 510(k) clearance on 2010-10-04. The listed applicant is Lumanosity, Inc.. The 510(k) number is K100213.

When did LUMANOSITY CELEBRITY, MODEL 204 receive FDA 510(k) clearance?

LUMANOSITY CELEBRITY, MODEL 204 received FDA 510(k) clearance on 2010-10-04, under 510(k) number K100213.

Who is the listed applicant for LUMANOSITY CELEBRITY, MODEL 204?

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

What is the FDA product code for LUMANOSITY CELEBRITY, MODEL 204?

The FDA product code for LUMANOSITY CELEBRITY, MODEL 204 is ILY.

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Official Source

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