VINYL EXAMINATION GLOVE, POWDERED
K-Number: K072223 · 2008-02-21
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Device Summary
Frequently Asked Questions
What is the VINYL EXAMINATION GLOVE, POWDERED?
VINYL EXAMINATION GLOVE, POWDERED is a medical device that received FDA 510(k) clearance on 2008-02-21. The listed applicant is Pinnacle Co., Ltd.. The 510(k) number is K072223.
When did VINYL EXAMINATION GLOVE, POWDERED receive FDA 510(k) clearance?
VINYL EXAMINATION GLOVE, POWDERED received FDA 510(k) clearance on 2008-02-21, under 510(k) number K072223.
Who is the listed applicant for VINYL EXAMINATION GLOVE, POWDERED?
The FDA 510(k) record lists Pinnacle Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINYL EXAMINATION GLOVE, POWDERED?
The FDA product code for VINYL EXAMINATION GLOVE, POWDERED 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 Pinnacle Co., Ltd. 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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