STERILE SURGEONS GLOVES -- MODIFICATION
K-Number: K922769 · 1992-10-06
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Device Summary
Frequently Asked Questions
What is the STERILE SURGEONS GLOVES -- MODIFICATION?
STERILE SURGEONS GLOVES -- MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-10-06. The listed applicant is Real Latex Pvt. , Ltd.. The 510(k) number is K922769.
When did STERILE SURGEONS GLOVES -- MODIFICATION receive FDA 510(k) clearance?
STERILE SURGEONS GLOVES -- MODIFICATION received FDA 510(k) clearance on 1992-10-06, under 510(k) number K922769.
Who is the listed applicant for STERILE SURGEONS GLOVES -- MODIFICATION?
The FDA 510(k) record lists Real Latex Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE SURGEONS GLOVES -- MODIFICATION?
The FDA product code for STERILE SURGEONS GLOVES -- MODIFICATION 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 Real Latex Pvt. , Ltd. 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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