POWDER FREE EXAMINATION GLOVE
K-Number: K915157 · 1993-02-02
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Device Summary
Frequently Asked Questions
What is the POWDER FREE EXAMINATION GLOVE?
POWDER FREE EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1993-02-02. The listed applicant is American Pro Latex, Inc.. The 510(k) number is K915157.
When did POWDER FREE EXAMINATION GLOVE receive FDA 510(k) clearance?
POWDER FREE EXAMINATION GLOVE received FDA 510(k) clearance on 1993-02-02, under 510(k) number K915157.
Who is the listed applicant for POWDER FREE EXAMINATION GLOVE?
The FDA 510(k) record lists American Pro Latex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE EXAMINATION GLOVE?
The FDA product code for POWDER FREE EXAMINATION 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.
Other records listing American Pro Latex, Inc. 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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