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FDA 510(k)

HEVEASHIELD EXAMINATION GLOVES

K-Number: K902700 · 1990-11-02

Decision Date1990-11-02
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEVEASHIELD EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Pacificlink Export. It received FDA 510(k) clearance on 1990-11-02 under 510(k) number K902700. 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 HEVEASHIELD EXAMINATION GLOVES?

HEVEASHIELD EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1990-11-02. The listed applicant is Pacificlink Export. The 510(k) number is K902700.

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

HEVEASHIELD EXAMINATION GLOVES received FDA 510(k) clearance on 1990-11-02, under 510(k) number K902700.

Who is the listed applicant for HEVEASHIELD EXAMINATION GLOVES?

The FDA 510(k) record lists Pacificlink Export as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEVEASHIELD EXAMINATION GLOVES?

The FDA product code for HEVEASHIELD 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 Pacificlink Export 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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