Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

POWDERED LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM)

K-Number: K993458 · 1999-11-10

Decision Date1999-11-10
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDERED LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM) 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 1999-11-10 under 510(k) number K993458. 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 POWDERED LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM)?

POWDERED LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM) is a medical device that received FDA 510(k) clearance on 1999-11-10. The listed applicant is Sri Johani Sdn. Bhd.. The 510(k) number is K993458.

When did POWDERED LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM) receive FDA 510(k) clearance?

POWDERED LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM) received FDA 510(k) clearance on 1999-11-10, under 510(k) number K993458.

Who is the listed applicant for POWDERED LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM)?

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 POWDERED LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM)?

The FDA product code for POWDERED LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM) 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.

↑