ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES, MODEL 87
K-Number: K003769 · 2000-12-22
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Device Summary
Frequently Asked Questions
What is the ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES, MODEL 87?
ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES, MODEL 87 is a medical device that received FDA 510(k) clearance on 2000-12-22. The listed applicant is Ansell Healthcare Products, Inc.. The 510(k) number is K003769.
When did ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES, MODEL 87 receive FDA 510(k) clearance?
ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES, MODEL 87 received FDA 510(k) clearance on 2000-12-22, under 510(k) number K003769.
Who is the listed applicant for ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES, MODEL 87?
The FDA 510(k) record lists Ansell Healthcare Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES, MODEL 87?
The FDA product code for ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES, MODEL 87 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 Ansell Healthcare Products, Inc. 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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