FDA 510(k)

SYNTHETIC POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES

K-Number: K990186 · 1999-06-21

ApplicantShanghai Intco. Plastic & Rubber Products Co., Ltd.

Decision Date1999-06-21

Product CodeLZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SYNTHETIC POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Intco. Plastic & Rubber Products Co., Ltd.. It received FDA 510(k) clearance on 1999-06-21 under 510(k) number K990186. 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 SYNTHETIC POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES?

SYNTHETIC POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1999-06-21. The listed applicant is Shanghai Intco. Plastic & Rubber Products Co., Ltd.. The 510(k) number is K990186.

When did SYNTHETIC POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

SYNTHETIC POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1999-06-21, under 510(k) number K990186.

Who is the listed applicant for SYNTHETIC POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES?

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

What is the FDA product code for SYNTHETIC POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES?

The FDA product code for SYNTHETIC POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES is LZA.

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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.