NON-STERILE LATEX PROCEDURE GLOVE
K-Number: K900869 · 1990-03-09
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Device Summary
Frequently Asked Questions
What is the NON-STERILE LATEX PROCEDURE GLOVE?
NON-STERILE LATEX PROCEDURE GLOVE is a medical device that received FDA 510(k) clearance on 1990-03-09. The listed applicant is Sri Johani Sdn. Bhd.. The 510(k) number is K900869.
When did NON-STERILE LATEX PROCEDURE GLOVE receive FDA 510(k) clearance?
NON-STERILE LATEX PROCEDURE GLOVE received FDA 510(k) clearance on 1990-03-09, under 510(k) number K900869.
Who is the listed applicant for NON-STERILE LATEX PROCEDURE GLOVE?
The FDA 510(k) record lists Sri Johani Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-STERILE LATEX PROCEDURE GLOVE?
The FDA product code for NON-STERILE LATEX PROCEDURE GLOVE is LYY.
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 Sri Johani Sdn. Bhd. 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: LYY)
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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