ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA
K-Number: K932664 · 1993-12-22
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Device Summary
Frequently Asked Questions
What is the ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA?
ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA is a medical device that received FDA 510(k) clearance on 1993-12-22. The listed applicant is Smith & Nephew Perry. The 510(k) number is K932664.
When did ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA receive FDA 510(k) clearance?
ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA received FDA 510(k) clearance on 1993-12-22, under 510(k) number K932664.
Who is the listed applicant for ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA?
The FDA 510(k) record lists Smith & Nephew Perry as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA?
The FDA product code for ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA 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 Smith & Nephew Perry 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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