POWDERFREE LATEX GLOVE
K-Number: K953986 · 1995-10-19
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Device Summary
Frequently Asked Questions
What is the POWDERFREE LATEX GLOVE?
POWDERFREE LATEX GLOVE is a medical device that received FDA 510(k) clearance on 1995-10-19. The listed applicant is Steriltx. The 510(k) number is K953986.
When did POWDERFREE LATEX GLOVE receive FDA 510(k) clearance?
POWDERFREE LATEX GLOVE received FDA 510(k) clearance on 1995-10-19, under 510(k) number K953986.
Who is the listed applicant for POWDERFREE LATEX GLOVE?
The FDA 510(k) record lists Steriltx as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDERFREE LATEX GLOVE?
The FDA product code for POWDERFREE LATEX GLOVE 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.
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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