VINYL EXAMINATION GLOVES (NON STERILE)
K-Number: K934536 · 1994-06-23
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Device Summary
Frequently Asked Questions
What is the VINYL EXAMINATION GLOVES (NON STERILE)?
VINYL EXAMINATION GLOVES (NON STERILE) is a medical device that received FDA 510(k) clearance on 1994-06-23. The listed applicant is Arista Latindo Industrial Ltd. P.T. The 510(k) number is K934536.
When did VINYL EXAMINATION GLOVES (NON STERILE) receive FDA 510(k) clearance?
VINYL EXAMINATION GLOVES (NON STERILE) received FDA 510(k) clearance on 1994-06-23, under 510(k) number K934536.
Who is the listed applicant for VINYL EXAMINATION GLOVES (NON STERILE)?
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 VINYL EXAMINATION GLOVES (NON STERILE)?
The FDA product code for VINYL EXAMINATION GLOVES (NON STERILE) 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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