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FDA 510(k)

ARG LATEX EXAMINATION GLOVES

K-Number: K891510 · 1989-04-28

Decision Date1989-04-28
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARG LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Palmbase Rubber Mfg. (M) Sdn Bhd. It received FDA 510(k) clearance on 1989-04-28 under 510(k) number K891510. 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 ARG LATEX EXAMINATION GLOVES?

ARG LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-28. The listed applicant is Palmbase Rubber Mfg. (M) Sdn Bhd. The 510(k) number is K891510.

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

ARG LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-04-28, under 510(k) number K891510.

Who is the listed applicant for ARG LATEX EXAMINATION GLOVES?

The FDA 510(k) record lists Palmbase Rubber Mfg. (M) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARG LATEX EXAMINATION GLOVES?

The FDA product code for ARG 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

View on FDA Database →

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

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