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FDA 510(k)

YOUNG AGAIN

K-Number: K124064 · 2013-12-19

ApplicantEspansione Marketing S.P.A
Decision Date2013-12-19
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

YOUNG AGAIN is the device name listed in this FDA 510(k) record. The listed applicant is Espansione Marketing S.P.A. It received FDA 510(k) clearance on 2013-12-19 under 510(k) number K124064. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YOUNG AGAIN?

YOUNG AGAIN is a medical device that received FDA 510(k) clearance on 2013-12-19. The listed applicant is Espansione Marketing S.P.A. The 510(k) number is K124064.

When did YOUNG AGAIN receive FDA 510(k) clearance?

YOUNG AGAIN received FDA 510(k) clearance on 2013-12-19, under 510(k) number K124064.

Who is the listed applicant for YOUNG AGAIN?

The FDA 510(k) record lists Espansione Marketing S.P.A as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YOUNG AGAIN?

The FDA product code for YOUNG AGAIN is OHS.

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Other records listing Espansione Marketing S.P.A as applicant

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.

K092734E-LIGHT LINEK070494EPI-C PLUS

Related Devices (Code: OHS)

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

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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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