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FDA 510(k)

BLUE LATEX EXAM GLOVES NON STERILE CHLORINATED POWDER FREE

K-Number: K073299 · 2008-03-05

Decision Date2008-03-05
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BLUE LATEX EXAM GLOVES NON STERILE CHLORINATED POWDER FREE is the device name listed in this FDA 510(k) record. The listed applicant is Betel Care Sdn. Bhd.. It received FDA 510(k) clearance on 2008-03-05 under 510(k) number K073299. 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 LATEX EXAM GLOVES NON STERILE CHLORINATED POWDER FREE?

BLUE LATEX EXAM GLOVES NON STERILE CHLORINATED POWDER FREE is a medical device that received FDA 510(k) clearance on 2008-03-05. The listed applicant is Betel Care Sdn. Bhd.. The 510(k) number is K073299.

When did BLUE LATEX EXAM GLOVES NON STERILE CHLORINATED POWDER FREE receive FDA 510(k) clearance?

BLUE LATEX EXAM GLOVES NON STERILE CHLORINATED POWDER FREE received FDA 510(k) clearance on 2008-03-05, under 510(k) number K073299.

Who is the listed applicant for BLUE LATEX EXAM GLOVES NON STERILE CHLORINATED POWDER FREE?

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

What is the FDA product code for BLUE LATEX EXAM GLOVES NON STERILE CHLORINATED POWDER FREE?

The FDA product code for BLUE LATEX EXAM GLOVES NON STERILE CHLORINATED 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 Betel Care 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.

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

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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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