STERILE NATURAL RUBBER LATEX SURGIONS' GLOVES
K-Number: K923576 · 1993-01-29
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Device Summary
Frequently Asked Questions
What is the STERILE NATURAL RUBBER LATEX SURGIONS' GLOVES?
STERILE NATURAL RUBBER LATEX SURGIONS' GLOVES is a medical device that received FDA 510(k) clearance on 1993-01-29. The listed applicant is Mri Corp.. The 510(k) number is K923576.
When did STERILE NATURAL RUBBER LATEX SURGIONS' GLOVES receive FDA 510(k) clearance?
STERILE NATURAL RUBBER LATEX SURGIONS' GLOVES received FDA 510(k) clearance on 1993-01-29, under 510(k) number K923576.
Who is the listed applicant for STERILE NATURAL RUBBER LATEX SURGIONS' GLOVES?
The FDA 510(k) record lists Mri Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE NATURAL RUBBER LATEX SURGIONS' GLOVES?
The FDA product code for STERILE NATURAL RUBBER LATEX SURGIONS' 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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