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FDA 510(k)

BLOSSOM POWDERED LATEX EXAMINATION GLOVES

K-Number: K984040 · 1999-01-13

Decision Date1999-01-13
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BLOSSOM POWDERED LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Mexpo Intl., Inc.. It received FDA 510(k) clearance on 1999-01-13 under 510(k) number K984040. 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 BLOSSOM POWDERED LATEX EXAMINATION GLOVES?

BLOSSOM POWDERED LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1999-01-13. The listed applicant is Mexpo Intl., Inc.. The 510(k) number is K984040.

When did BLOSSOM POWDERED LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?

BLOSSOM POWDERED LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1999-01-13, under 510(k) number K984040.

Who is the listed applicant for BLOSSOM POWDERED LATEX EXAMINATION GLOVES?

The FDA 510(k) record lists Mexpo Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOSSOM POWDERED LATEX EXAMINATION GLOVES?

The FDA product code for BLOSSOM POWDERED 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.

Other records listing Mexpo Intl., Inc. 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.

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

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