MODERN LATEX STERILE SURGICAL GLOVES
K-Number: K890073 · 1989-01-24
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Device Summary
Frequently Asked Questions
What is the MODERN LATEX STERILE SURGICAL GLOVES?
MODERN LATEX STERILE SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1989-01-24. The listed applicant is Modern Rubber Co., Ltd. C/O World Trade Svc.. The 510(k) number is K890073.
When did MODERN LATEX STERILE SURGICAL GLOVES receive FDA 510(k) clearance?
MODERN LATEX STERILE SURGICAL GLOVES received FDA 510(k) clearance on 1989-01-24, under 510(k) number K890073.
Who is the listed applicant for MODERN LATEX STERILE SURGICAL GLOVES?
The FDA 510(k) record lists Modern Rubber Co., Ltd. C/O World Trade Svc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODERN LATEX STERILE SURGICAL GLOVES?
The FDA product code for MODERN LATEX STERILE SURGICAL 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.
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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