FDA 510(k)

LATEX EXAMINATION GLOVES, NON-STERILE

K-Number: K891365 · 1989-04-26

ApplicantChina National Medicines & Health Prod. I/E Corp.

Decision Date1989-04-26

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

LATEX EXAMINATION GLOVES, NON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is China National Medicines & Health Prod. I/E Corp.. It received FDA 510(k) clearance on 1989-04-26 under 510(k) number K891365. 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 LATEX EXAMINATION GLOVES, NON-STERILE?

LATEX EXAMINATION GLOVES, NON-STERILE is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is China National Medicines & Health Prod. I/E Corp.. The 510(k) number is K891365.

When did LATEX EXAMINATION GLOVES, NON-STERILE receive FDA 510(k) clearance?

LATEX EXAMINATION GLOVES, NON-STERILE received FDA 510(k) clearance on 1989-04-26, under 510(k) number K891365.

Who is the listed applicant for LATEX EXAMINATION GLOVES, NON-STERILE?

The FDA 510(k) record lists China National Medicines & Health Prod. I/E Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX EXAMINATION GLOVES, NON-STERILE?

The FDA product code for LATEX EXAMINATION GLOVES, NON-STERILE is LYY.

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Other records listing China National Medicines & Health Prod. I/E Corp. as applicant

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Related Devices (Code: LYY)

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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.