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)

BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE

K-Number: K062527 · 2007-02-20

Decision Date2007-02-20
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Multisafe Sdn. Bhd.. It received FDA 510(k) clearance on 2007-02-20 under 510(k) number K062527. 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 BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE?

BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE is a medical device that received FDA 510(k) clearance on 2007-02-20. The listed applicant is Multisafe Sdn. Bhd.. The 510(k) number is K062527.

When did BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE receive FDA 510(k) clearance?

BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE received FDA 510(k) clearance on 2007-02-20, under 510(k) number K062527.

Who is the listed applicant for BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE?

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

What is the FDA product code for BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE?

The FDA product code for BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE 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 Multisafe 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 8 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.

↑