BIOGEL LATEX STERILE POWDER-FREE GLOVE
K-Number: K050899 · 2005-08-12
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Device Summary
Frequently Asked Questions
What is the BIOGEL LATEX STERILE POWDER-FREE GLOVE?
BIOGEL LATEX STERILE POWDER-FREE GLOVE is a medical device that received FDA 510(k) clearance on 2005-08-12. The listed applicant is Regent Medical Americas, LLC. The 510(k) number is K050899.
When did BIOGEL LATEX STERILE POWDER-FREE GLOVE receive FDA 510(k) clearance?
BIOGEL LATEX STERILE POWDER-FREE GLOVE received FDA 510(k) clearance on 2005-08-12, under 510(k) number K050899.
Who is the listed applicant for BIOGEL LATEX STERILE POWDER-FREE GLOVE?
The FDA 510(k) record lists Regent Medical Americas, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOGEL LATEX STERILE POWDER-FREE GLOVE?
The FDA product code for BIOGEL LATEX STERILE POWDER-FREE GLOVE 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 Regent Medical Americas, LLC 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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