SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE)
K-Number: K072228 · 2008-02-08
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Device Summary
Frequently Asked Questions
What is the SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE)?
SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE) is a medical device that received FDA 510(k) clearance on 2008-02-08. The listed applicant is Pinnacle Co., Ltd.. The 510(k) number is K072228.
When did SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE) receive FDA 510(k) clearance?
SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE) received FDA 510(k) clearance on 2008-02-08, under 510(k) number K072228.
Who is the listed applicant for SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE)?
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 SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE)?
The FDA product code for SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE) 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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