LATEX SURGEONS GLOVE (POWDER FREE)
K-Number: K014283 · 2002-05-22
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Device Summary
Frequently Asked Questions
What is the LATEX SURGEONS GLOVE (POWDER FREE)?
LATEX SURGEONS GLOVE (POWDER FREE) is a medical device that received FDA 510(k) clearance on 2002-05-22. The listed applicant is Brightway Gloves Pvt. , Ltd.. The 510(k) number is K014283.
When did LATEX SURGEONS GLOVE (POWDER FREE) receive FDA 510(k) clearance?
LATEX SURGEONS GLOVE (POWDER FREE) received FDA 510(k) clearance on 2002-05-22, under 510(k) number K014283.
Who is the listed applicant for LATEX SURGEONS GLOVE (POWDER FREE)?
The FDA 510(k) record lists Brightway Gloves Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX SURGEONS GLOVE (POWDER FREE)?
The FDA product code for LATEX SURGEONS GLOVE (POWDER FREE) 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 Brightway Gloves Pvt. , Ltd. 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: 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
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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