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FDA 510(k)

PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER

K-Number: K893782 · 1989-07-14

Decision Date1989-07-14
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER is the device name listed in this FDA 510(k) record. The listed applicant is Rubberex (M) Sdn Berhad. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K893782. 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 PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER?

PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Rubberex (M) Sdn Berhad. The 510(k) number is K893782.

When did PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER receive FDA 510(k) clearance?

PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893782.

Who is the listed applicant for PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER?

The FDA 510(k) record lists Rubberex (M) Sdn Berhad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER?

The FDA product code for PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER 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 Rubberex (M) Sdn Berhad 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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