LATEX SURGICAL GLOVE
K-Number: K881664 · 1989-01-06
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Device Summary
Frequently Asked Questions
What is the LATEX SURGICAL GLOVE?
LATEX SURGICAL GLOVE is a medical device that received FDA 510(k) clearance on 1989-01-06. The listed applicant is Lien Chang Rubber Industrial Co., Ltd.. The 510(k) number is K881664.
When did LATEX SURGICAL GLOVE receive FDA 510(k) clearance?
LATEX SURGICAL GLOVE received FDA 510(k) clearance on 1989-01-06, under 510(k) number K881664.
Who is the listed applicant for LATEX SURGICAL GLOVE?
The FDA 510(k) record lists Lien Chang 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 GLOVE?
The FDA product code for LATEX SURGICAL GLOVE 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 Lien Chang 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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