ANSELL NO POWDER SURGEON'S GLOVES
K-Number: K850635 · 1985-06-26
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Device Summary
Frequently Asked Questions
What is the ANSELL NO POWDER SURGEON'S GLOVES?
ANSELL NO POWDER SURGEON'S GLOVES is a medical device that received FDA 510(k) clearance on 1985-06-26. The listed applicant is Ansell, Inc.. The 510(k) number is K850635.
When did ANSELL NO POWDER SURGEON'S GLOVES receive FDA 510(k) clearance?
ANSELL NO POWDER SURGEON'S GLOVES received FDA 510(k) clearance on 1985-06-26, under 510(k) number K850635.
Who is the listed applicant for ANSELL NO POWDER SURGEON'S GLOVES?
The FDA 510(k) record lists Ansell, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANSELL NO POWDER SURGEON'S GLOVES?
The FDA product code for ANSELL NO POWDER SURGEON'S GLOVES 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, 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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