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FDA 510(k)

G-DERM POWDER-FREE SYNTHETIC SURGICAL GLOVE

K-Number: K121335 · 2012-09-13

Decision Date2012-09-13
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

G-DERM POWDER-FREE SYNTHETIC SURGICAL GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Hutchinson Sante S.N.C.. It received FDA 510(k) clearance on 2012-09-13 under 510(k) number K121335. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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