ACCUMED LATEX SURGICAL GLOVE
K-Number: K893834 · 1989-12-14
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Device Summary
Frequently Asked Questions
What is the ACCUMED LATEX SURGICAL GLOVE?
ACCUMED LATEX SURGICAL GLOVE is a medical device that received FDA 510(k) clearance on 1989-12-14. The listed applicant is Accurate Medical Devices, Inc.. The 510(k) number is K893834.
When did ACCUMED LATEX SURGICAL GLOVE receive FDA 510(k) clearance?
ACCUMED LATEX SURGICAL GLOVE received FDA 510(k) clearance on 1989-12-14, under 510(k) number K893834.
Who is the listed applicant for ACCUMED LATEX SURGICAL GLOVE?
The FDA 510(k) record lists Accurate Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACCUMED LATEX SURGICAL GLOVE?
The FDA product code for ACCUMED LATEX 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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