G-DERM POWDER-FREE SYNTHETIC SURGICAL GLOVE
K-Number: K121335 · 2012-09-13
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Device Summary
Frequently Asked Questions
What is the G-DERM POWDER-FREE SYNTHETIC SURGICAL GLOVE?
G-DERM POWDER-FREE SYNTHETIC SURGICAL GLOVE is a medical device that received FDA 510(k) clearance on 2012-09-13. The listed applicant is Hutchinson Sante S.N.C.. The 510(k) number is K121335.
When did G-DERM POWDER-FREE SYNTHETIC SURGICAL GLOVE receive FDA 510(k) clearance?
G-DERM POWDER-FREE SYNTHETIC SURGICAL GLOVE received FDA 510(k) clearance on 2012-09-13, under 510(k) number K121335.
Who is the listed applicant for G-DERM POWDER-FREE SYNTHETIC SURGICAL GLOVE?
The FDA 510(k) record lists Hutchinson Sante S.N.C. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for G-DERM POWDER-FREE SYNTHETIC SURGICAL GLOVE?
The FDA product code for G-DERM POWDER-FREE SYNTHETIC SURGICAL 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.
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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