LATEX SURGICAL GLOVES,STERILE/NON STERILE MOD BRAN
K-Number: K892064 · 1989-04-26
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Device Summary
Frequently Asked Questions
What is the LATEX SURGICAL GLOVES,STERILE/NON STERILE MOD BRAN?
LATEX SURGICAL GLOVES,STERILE/NON STERILE MOD BRAN is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is Modern Rubber Industrial Co., Ltd.. The 510(k) number is K892064.
When did LATEX SURGICAL GLOVES,STERILE/NON STERILE MOD BRAN receive FDA 510(k) clearance?
LATEX SURGICAL GLOVES,STERILE/NON STERILE MOD BRAN received FDA 510(k) clearance on 1989-04-26, under 510(k) number K892064.
Who is the listed applicant for LATEX SURGICAL GLOVES,STERILE/NON STERILE MOD BRAN?
The FDA 510(k) record lists Modern Rubber Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX SURGICAL GLOVES,STERILE/NON STERILE MOD BRAN?
The FDA product code for LATEX SURGICAL GLOVES,STERILE/NON STERILE MOD BRAN 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 Modern Rubber Industrial Co., 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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