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FDA 510(k)

ULTRA BEAUTY

K-Number: K112351 · 2012-03-30

ApplicantJohari Digital Healthcare , Ltd.
Decision Date2012-03-30
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ULTRA BEAUTY is the device name listed in this FDA 510(k) record. The listed applicant is Johari Digital Healthcare , Ltd.. It received FDA 510(k) clearance on 2012-03-30 under 510(k) number K112351. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA BEAUTY?

ULTRA BEAUTY is a medical device that received FDA 510(k) clearance on 2012-03-30. The listed applicant is Johari Digital Healthcare , Ltd.. The 510(k) number is K112351.

When did ULTRA BEAUTY receive FDA 510(k) clearance?

ULTRA BEAUTY received FDA 510(k) clearance on 2012-03-30, under 510(k) number K112351.

Who is the listed applicant for ULTRA BEAUTY?

The FDA 510(k) record lists Johari Digital Healthcare , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRA BEAUTY?

The FDA product code for ULTRA BEAUTY is NFO.

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Other records listing Johari Digital Healthcare , Ltd. as applicant

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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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