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FDA 510(k)

POWDER FREE STERILE LATEX SURGICAL GLOVES

K-Number: K052177 · 2005-12-09

Decision Date2005-12-09
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POWDER FREE STERILE LATEX SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Hartalega Sdn Bhd. It received FDA 510(k) clearance on 2005-12-09 under 510(k) number K052177. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWDER FREE STERILE LATEX SURGICAL GLOVES?

POWDER FREE STERILE LATEX SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 2005-12-09. The listed applicant is Hartalega Sdn Bhd. The 510(k) number is K052177.

When did POWDER FREE STERILE LATEX SURGICAL GLOVES receive FDA 510(k) clearance?

POWDER FREE STERILE LATEX SURGICAL GLOVES received FDA 510(k) clearance on 2005-12-09, under 510(k) number K052177.

Who is the listed applicant for POWDER FREE STERILE LATEX SURGICAL GLOVES?

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

What is the FDA product code for POWDER FREE STERILE LATEX SURGICAL GLOVES?

The FDA product code for POWDER FREE STERILE LATEX SURGICAL GLOVES is KGO.

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 Hartalega 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 55 devices →

Related Devices (Code: KGO)

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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