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FDA 510(k)

L-SER KO LAMP

K-Number: K112016 · 2012-02-10

ApplicantYa-Man, Ltd.
Decision Date2012-02-10
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

L-SER KO LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Ya-Man, Ltd.. It received FDA 510(k) clearance on 2012-02-10 under 510(k) number K112016. 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 L-SER KO LAMP?

L-SER KO LAMP is a medical device that received FDA 510(k) clearance on 2012-02-10. The listed applicant is Ya-Man, Ltd.. The 510(k) number is K112016.

When did L-SER KO LAMP receive FDA 510(k) clearance?

L-SER KO LAMP received FDA 510(k) clearance on 2012-02-10, under 510(k) number K112016.

Who is the listed applicant for L-SER KO LAMP?

The FDA 510(k) record lists Ya-Man, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L-SER KO LAMP?

The FDA product code for L-SER KO LAMP is ILY.

Other records listing Ya-Man, Ltd. 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.

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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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