LATEX EXAM GLOVES
K-Number: K893241 · 1989-07-14
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Device Summary
Frequently Asked Questions
What is the LATEX EXAM GLOVES?
LATEX EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Semodal Jaya Sdn. Bhd.. The 510(k) number is K893241.
When did LATEX EXAM GLOVES receive FDA 510(k) clearance?
LATEX EXAM GLOVES received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893241.
Who is the listed applicant for LATEX EXAM GLOVES?
The FDA 510(k) record lists Semodal Jaya Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX EXAM GLOVES?
The FDA product code for LATEX EXAM GLOVES 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 Semodal Jaya 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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