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FDA 510(k)

HARCROS EXAMINATION GLOVES

K-Number: K893823 · 1989-08-29

ApplicantH&C Rubber Products Sdn. Bhd.
Decision Date1989-08-29
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HARCROS EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is H&C Rubber Products Sdn. Bhd.. It received FDA 510(k) clearance on 1989-08-29 under 510(k) number K893823. 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 HARCROS EXAMINATION GLOVES?

HARCROS EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-29. The listed applicant is H&C Rubber Products Sdn. Bhd.. The 510(k) number is K893823.

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

HARCROS EXAMINATION GLOVES received FDA 510(k) clearance on 1989-08-29, under 510(k) number K893823.

Who is the listed applicant for HARCROS EXAMINATION GLOVES?

The FDA 510(k) record lists H&C Rubber Products Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HARCROS EXAMINATION GLOVES?

The FDA product code for HARCROS EXAMINATION GLOVES is LYY.

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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.

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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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