POWDERFREE NATURAL LATEX GLOVES
K-Number: K921389 · 1993-08-05
Advertisement
Device Summary
Frequently Asked Questions
What is the POWDERFREE NATURAL LATEX GLOVES?
POWDERFREE NATURAL LATEX GLOVES is a medical device that received FDA 510(k) clearance on 1993-08-05. The listed applicant is Arista Latindo Industrial Ltd. P.T. The 510(k) number is K921389.
When did POWDERFREE NATURAL LATEX GLOVES receive FDA 510(k) clearance?
POWDERFREE NATURAL LATEX GLOVES received FDA 510(k) clearance on 1993-08-05, under 510(k) number K921389.
Who is the listed applicant for POWDERFREE NATURAL LATEX 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 POWDERFREE NATURAL LATEX GLOVES?
The FDA product code for POWDERFREE NATURAL LATEX 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 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: 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.
Advertisement