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FDA 510(k)

STERILE LATEX EXAMINATION GLOVE

K-Number: K900868 · 1990-03-09

Decision Date1990-03-09
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE LATEX EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Sri Johani Sdn. Bhd.. It received FDA 510(k) clearance on 1990-03-09 under 510(k) number K900868. 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 STERILE LATEX EXAMINATION GLOVE?

STERILE LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1990-03-09. The listed applicant is Sri Johani Sdn. Bhd.. The 510(k) number is K900868.

When did STERILE LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?

STERILE LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1990-03-09, under 510(k) number K900868.

Who is the listed applicant for STERILE LATEX EXAMINATION GLOVE?

The FDA 510(k) record lists Sri Johani Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE LATEX EXAMINATION GLOVE?

The FDA product code for STERILE LATEX EXAMINATION GLOVE 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 Sri Johani Sdn. Bhd. 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.

View all 23 devices →

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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