ARISTA VINYL EXAMINATION GLOVES
K-Number: K954153 · 1996-01-26
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Device Summary
Frequently Asked Questions
What is the ARISTA VINYL EXAMINATION GLOVES?
ARISTA VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1996-01-26. The listed applicant is Arista Latindo Industrial Ltd. P.T. The 510(k) number is K954153.
When did ARISTA VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?
ARISTA VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 1996-01-26, under 510(k) number K954153.
Who is the listed applicant for ARISTA VINYL EXAMINATION GLOVES?
The FDA 510(k) record lists Arista Latindo Industrial Ltd. P.T as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARISTA VINYL EXAMINATION GLOVES?
The FDA product code for ARISTA VINYL EXAMINATION GLOVES is LYZ.
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 Arista Latindo Industrial Ltd. P.T 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: LYZ)
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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