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FDA 510(k)

CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES

K-Number: K991155 · 1999-06-21

Decision Date1999-06-21
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is C.V. Anlis Abadi International. It received FDA 510(k) clearance on 1999-06-21 under 510(k) number K991155. 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 CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES?

CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1999-06-21. The listed applicant is C.V. Anlis Abadi International. The 510(k) number is K991155.

When did CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?

CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1999-06-21, under 510(k) number K991155.

Who is the listed applicant for CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES?

The FDA 510(k) record lists C.V. Anlis Abadi International as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES?

The FDA product code for CHLORINATED POWDER FREE LATEX EXAMINATION 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.

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

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