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FDA 510(k)

PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES

K-Number: K992676 · 1999-12-16

Decision Date1999-12-16
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Wear Safe Malaysia Sdn. Bhd.. It received FDA 510(k) clearance on 1999-12-16 under 510(k) number K992676. 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 PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES?

PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES is a medical device that received FDA 510(k) clearance on 1999-12-16. The listed applicant is Wear Safe Malaysia Sdn. Bhd.. The 510(k) number is K992676.

When did PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES receive FDA 510(k) clearance?

PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES received FDA 510(k) clearance on 1999-12-16, under 510(k) number K992676.

Who is the listed applicant for PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES?

The FDA 510(k) record lists Wear Safe Malaysia Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES?

The FDA product code for PATIENT LATEX EXAMINATION POWDER-FREE POLYMER COATED GLOVES is LYY.

Related Clinical Trials

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.

Other records listing Wear Safe Malaysia Sdn. Bhd. as applicant

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.

View all 14 devices →

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.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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