LATEX SURGICAL STERILE GLOVES
K-Number: K903212 · 1990-08-01
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Device Summary
Frequently Asked Questions
What is the LATEX SURGICAL STERILE GLOVES?
LATEX SURGICAL STERILE GLOVES is a medical device that received FDA 510(k) clearance on 1990-08-01. The listed applicant is Mirage Medical & Chemical, Inc.. The 510(k) number is K903212.
When did LATEX SURGICAL STERILE GLOVES receive FDA 510(k) clearance?
LATEX SURGICAL STERILE GLOVES received FDA 510(k) clearance on 1990-08-01, under 510(k) number K903212.
Who is the listed applicant for LATEX SURGICAL STERILE GLOVES?
The FDA 510(k) record lists Mirage Medical & Chemical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX SURGICAL STERILE GLOVES?
The FDA product code for LATEX SURGICAL STERILE 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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