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FDA 510(k)

PLASTIC (VINYL) EXAMINATION GLOVES

K-Number: K910879 · 1991-04-25

Decision Date1991-04-25
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PLASTIC (VINYL) EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Siamount Plastic Corporation , Ltd.. It received FDA 510(k) clearance on 1991-04-25 under 510(k) number K910879. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASTIC (VINYL) EXAMINATION GLOVES?

PLASTIC (VINYL) EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1991-04-25. The listed applicant is Siamount Plastic Corporation , Ltd.. The 510(k) number is K910879.

When did PLASTIC (VINYL) EXAMINATION GLOVES receive FDA 510(k) clearance?

PLASTIC (VINYL) EXAMINATION GLOVES received FDA 510(k) clearance on 1991-04-25, under 510(k) number K910879.

Who is the listed applicant for PLASTIC (VINYL) EXAMINATION GLOVES?

The FDA 510(k) record lists Siamount Plastic Corporation , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLASTIC (VINYL) EXAMINATION GLOVES?

The FDA product code for PLASTIC (VINYL) EXAMINATION GLOVES is LYZ.

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: LYZ)

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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