FDA 510(k)

SHARPS CONTAINER

K-Number: K101567 · 2010-09-02

Decision Date2010-09-02

Product CodeMMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SHARPS CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Cixi Leinuo Plastic Co., Ltd.. It received FDA 510(k) clearance on 2010-09-02 under 510(k) number K101567. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARPS CONTAINER?

SHARPS CONTAINER is a medical device that received FDA 510(k) clearance on 2010-09-02. The listed applicant is Cixi Leinuo Plastic Co., Ltd.. The 510(k) number is K101567.

When did SHARPS CONTAINER receive FDA 510(k) clearance?

SHARPS CONTAINER received FDA 510(k) clearance on 2010-09-02, under 510(k) number K101567.

Who is the listed applicant for SHARPS CONTAINER?

The FDA 510(k) record lists Cixi Leinuo Plastic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHARPS CONTAINER?

The FDA product code for SHARPS CONTAINER is MMK.

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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.