SAS RUBBER PRODUCTS CO./LATEX EXAMINATION GLOVES
K-Number: K911939 · 1991-11-15
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Device Summary
Frequently Asked Questions
What is the SAS RUBBER PRODUCTS CO./LATEX EXAMINATION GLOVES?
SAS RUBBER PRODUCTS CO./LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1991-11-15. The listed applicant is Overseas Import & Export Dist.. The 510(k) number is K911939.
When did SAS RUBBER PRODUCTS CO./LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
SAS RUBBER PRODUCTS CO./LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1991-11-15, under 510(k) number K911939.
Who is the listed applicant for SAS RUBBER PRODUCTS CO./LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Overseas Import & Export Dist. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAS RUBBER PRODUCTS CO./LATEX EXAMINATION GLOVES?
The FDA product code for SAS RUBBER PRODUCTS CO./LATEX EXAMINATION GLOVES 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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