POWDER-FREE LATEX EXAMINATION GLOVE
K-Number: K952473 · 1995-10-12
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Device Summary
Frequently Asked Questions
What is the POWDER-FREE LATEX EXAMINATION GLOVE?
POWDER-FREE LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1995-10-12. The listed applicant is M.M.R. Gloves Private , Ltd.. The 510(k) number is K952473.
When did POWDER-FREE LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?
POWDER-FREE LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1995-10-12, under 510(k) number K952473.
Who is the listed applicant for POWDER-FREE LATEX EXAMINATION GLOVE?
The FDA 510(k) record lists M.M.R. Gloves Private , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER-FREE LATEX EXAMINATION GLOVE?
The FDA product code for POWDER-FREE LATEX EXAMINATION GLOVE 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.
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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