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)

LATEX EXAMINATION GLOVE POWDER FREE

K-Number: K974870 · 1998-03-13

Decision Date1998-03-13
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAMINATION GLOVE POWDER FREE is the device name listed in this FDA 510(k) record. The listed applicant is Smart Glove Corp. Sdn Bhd. It received FDA 510(k) clearance on 1998-03-13 under 510(k) number K974870. 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 LATEX EXAMINATION GLOVE POWDER FREE?

LATEX EXAMINATION GLOVE POWDER FREE is a medical device that received FDA 510(k) clearance on 1998-03-13. The listed applicant is Smart Glove Corp. Sdn Bhd. The 510(k) number is K974870.

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

LATEX EXAMINATION GLOVE POWDER FREE received FDA 510(k) clearance on 1998-03-13, under 510(k) number K974870.

Who is the listed applicant for LATEX EXAMINATION GLOVE POWDER FREE?

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

What is the FDA product code for LATEX EXAMINATION GLOVE POWDER FREE?

The FDA product code for LATEX EXAMINATION GLOVE POWDER FREE 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 Smart Glove Corp. 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 27 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.

↑