BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE
K-Number: K053442 · 2006-03-07
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Device Summary
Frequently Asked Questions
What is the BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE?
BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE is a medical device that received FDA 510(k) clearance on 2006-03-07. The listed applicant is Regent Medical Americas, LLC. The 510(k) number is K053442.
When did BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE receive FDA 510(k) clearance?
BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE received FDA 510(k) clearance on 2006-03-07, under 510(k) number K053442.
Who is the listed applicant for BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX 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 SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE?
The FDA product code for BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX 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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