FDA 510(k)

NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE

K-Number: K001128 · 2000-05-23

ApplicantShanghai Poseidon Plastic Products Co., Ltd.

Decision Date2000-05-23

Product CodeLZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Poseidon Plastic Products Co., Ltd.. It received FDA 510(k) clearance on 2000-05-23 under 510(k) number K001128. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE?

NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE is a medical device that received FDA 510(k) clearance on 2000-05-23. The listed applicant is Shanghai Poseidon Plastic Products Co., Ltd.. The 510(k) number is K001128.

When did NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE receive FDA 510(k) clearance?

NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE received FDA 510(k) clearance on 2000-05-23, under 510(k) number K001128.

Who is the listed applicant for NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE?

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

What is the FDA product code for NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE?

The FDA product code for NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE is LZA.

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Other records listing Shanghai Poseidon Plastic Products Co., Ltd. as applicant

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Related Devices (Code: LZA)

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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.