FDA 510(k)

MULTIPLE PRIVATE LABELS, NITRILE EXAM GLOVES, POWDER-FREE (WHITE)

K-Number: K001549 · 2000-06-12

ApplicantShanghai Poseidon Plastic Products Co., Ltd.

Decision Date2000-06-12

Product CodeLZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MULTIPLE PRIVATE LABELS, NITRILE EXAM GLOVES, POWDER-FREE (WHITE) 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 2000-06-12 under 510(k) number K001549. 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 MULTIPLE PRIVATE LABELS, NITRILE EXAM GLOVES, POWDER-FREE (WHITE)?

MULTIPLE PRIVATE LABELS, NITRILE EXAM GLOVES, POWDER-FREE (WHITE) is a medical device that received FDA 510(k) clearance on 2000-06-12. The listed applicant is Shanghai Poseidon Plastic Products Co., Ltd.. The 510(k) number is K001549.

When did MULTIPLE PRIVATE LABELS, NITRILE EXAM GLOVES, POWDER-FREE (WHITE) receive FDA 510(k) clearance?

MULTIPLE PRIVATE LABELS, NITRILE EXAM GLOVES, POWDER-FREE (WHITE) received FDA 510(k) clearance on 2000-06-12, under 510(k) number K001549.

Who is the listed applicant for MULTIPLE PRIVATE LABELS, NITRILE EXAM GLOVES, POWDER-FREE (WHITE)?

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 MULTIPLE PRIVATE LABELS, NITRILE EXAM GLOVES, POWDER-FREE (WHITE)?

The FDA product code for MULTIPLE PRIVATE LABELS, NITRILE EXAM GLOVES, POWDER-FREE (WHITE) 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.