POWDER-FREE LATEX EXAMINATION GLOVE, BLUE COLORED
K-Number: K011271 · 2001-05-08
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Device Summary
Frequently Asked Questions
What is the POWDER-FREE LATEX EXAMINATION GLOVE, BLUE COLORED?
POWDER-FREE LATEX EXAMINATION GLOVE, BLUE COLORED is a medical device that received FDA 510(k) clearance on 2001-05-08. The listed applicant is Perusahaan Getah Asas Sdn. Bhd.. The 510(k) number is K011271.
When did POWDER-FREE LATEX EXAMINATION GLOVE, BLUE COLORED receive FDA 510(k) clearance?
POWDER-FREE LATEX EXAMINATION GLOVE, BLUE COLORED received FDA 510(k) clearance on 2001-05-08, under 510(k) number K011271.
Who is the listed applicant for POWDER-FREE LATEX EXAMINATION GLOVE, BLUE COLORED?
The FDA 510(k) record lists Perusahaan Getah Asas Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER-FREE LATEX EXAMINATION GLOVE, BLUE COLORED?
The FDA product code for POWDER-FREE LATEX EXAMINATION GLOVE, BLUE COLORED 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 Perusahaan Getah Asas 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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