STERILE SURGEONS' GLOVES
K-Number: K891621 · 1989-04-20
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Device Summary
Frequently Asked Questions
What is the STERILE SURGEONS' GLOVES?
STERILE SURGEONS' GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-20. The listed applicant is Albors-Menconi Latex Corp.. The 510(k) number is K891621.
When did STERILE SURGEONS' GLOVES receive FDA 510(k) clearance?
STERILE SURGEONS' GLOVES received FDA 510(k) clearance on 1989-04-20, under 510(k) number K891621.
Who is the listed applicant for STERILE SURGEONS' GLOVES?
The FDA 510(k) record lists Albors-Menconi Latex Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE SURGEONS' GLOVES?
The FDA product code for STERILE SURGEONS' 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 Albors-Menconi Latex Corp. 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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