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FDA 510(k)

LIFE4C

K-Number: K063304 · 2007-12-21

ApplicantNumedis, Inc.
Decision Date2007-12-21
Product CodeLYX
DecisionSubstantially Equivalent

Device Summary

LIFE4C is the device name listed in this FDA 510(k) record. The listed applicant is Numedis, Inc.. It received FDA 510(k) clearance on 2007-12-21 under 510(k) number K063304. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE4C?

LIFE4C is a medical device that received FDA 510(k) clearance on 2007-12-21. The listed applicant is Numedis, Inc.. The 510(k) number is K063304.

When did LIFE4C receive FDA 510(k) clearance?

LIFE4C received FDA 510(k) clearance on 2007-12-21, under 510(k) number K063304.

Who is the listed applicant for LIFE4C?

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

What is the FDA product code for LIFE4C?

The FDA product code for LIFE4C is LYX.

Related Devices (Code: LYX)

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.

K251320XTRA4Al.Chi.Mi.A. S.R.LK221759CornisolAurolabK211786Independent Corneal Viewing Chamber (IVC-21)Bausch + Lomb, IncorporatedK162013Eusol-CAl.Chi.Mi.A. S.R.LK063617EUSOL-CAl.Chi.Mi.AK032422EUSOL-CAl.Chi.Mi.A

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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