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FDA 510(k)

YA MEI FIRST AID KIT

K-Number: K031130 · 2003-06-27

ApplicantYa Mei Technology Co., Ltd.
Decision Date2003-06-27
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

YA MEI FIRST AID KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ya Mei Technology Co., Ltd.. It received FDA 510(k) clearance on 2003-06-27 under 510(k) number K031130. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YA MEI FIRST AID KIT?

YA MEI FIRST AID KIT is a medical device that received FDA 510(k) clearance on 2003-06-27. The listed applicant is Ya Mei Technology Co., Ltd.. The 510(k) number is K031130.

When did YA MEI FIRST AID KIT receive FDA 510(k) clearance?

YA MEI FIRST AID KIT received FDA 510(k) clearance on 2003-06-27, under 510(k) number K031130.

Who is the listed applicant for YA MEI FIRST AID KIT?

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

What is the FDA product code for YA MEI FIRST AID KIT?

The FDA product code for YA MEI FIRST AID KIT is KGO.

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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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