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FDA 510(k)

SINOCHEM NINGBO LATEX EXAMINATION GLOVE, POWDER FREE

K-Number: K955918 · 1996-06-27

ApplicantSinochem Ningbo Imp & Exp Corp.
Decision Date1996-06-27
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SINOCHEM NINGBO LATEX EXAMINATION GLOVE, POWDER FREE is the device name listed in this FDA 510(k) record. The listed applicant is Sinochem Ningbo Imp & Exp Corp.. It received FDA 510(k) clearance on 1996-06-27 under 510(k) number K955918. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINOCHEM NINGBO LATEX EXAMINATION GLOVE, POWDER FREE?

SINOCHEM NINGBO LATEX EXAMINATION GLOVE, POWDER FREE is a medical device that received FDA 510(k) clearance on 1996-06-27. The listed applicant is Sinochem Ningbo Imp & Exp Corp.. The 510(k) number is K955918.

When did SINOCHEM NINGBO LATEX EXAMINATION GLOVE, POWDER FREE receive FDA 510(k) clearance?

SINOCHEM NINGBO LATEX EXAMINATION GLOVE, POWDER FREE received FDA 510(k) clearance on 1996-06-27, under 510(k) number K955918.

Who is the listed applicant for SINOCHEM NINGBO LATEX EXAMINATION GLOVE, POWDER FREE?

The FDA 510(k) record lists Sinochem Ningbo Imp & Exp Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SINOCHEM NINGBO LATEX EXAMINATION GLOVE, POWDER FREE?

The FDA product code for SINOCHEM NINGBO LATEX EXAMINATION GLOVE, POWDER FREE is LYY.

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Related Devices (Code: LYY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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