DR. BOO POWDER-FREE LATEX EXAM GLOVES
K-Number: K941240 · 1994-06-21
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Device Summary
Frequently Asked Questions
What is the DR. BOO POWDER-FREE LATEX EXAM GLOVES?
DR. BOO POWDER-FREE LATEX EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1994-06-21. The listed applicant is Dr. Boo Co., Ltd.. The 510(k) number is K941240.
When did DR. BOO POWDER-FREE LATEX EXAM GLOVES receive FDA 510(k) clearance?
DR. BOO POWDER-FREE LATEX EXAM GLOVES received FDA 510(k) clearance on 1994-06-21, under 510(k) number K941240.
Who is the listed applicant for DR. BOO POWDER-FREE LATEX EXAM GLOVES?
The FDA 510(k) record lists Dr. Boo Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DR. BOO POWDER-FREE LATEX EXAM GLOVES?
The FDA product code for DR. BOO POWDER-FREE LATEX EXAM 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.
Other records listing Dr. Boo Co., 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: 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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