POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES
K-Number: K022600 · 2002-09-16
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Device Summary
Frequently Asked Questions
What is the POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES?
POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2002-09-16. The listed applicant is Shijiazhuang Wally Plastics Co., Ltd.. The 510(k) number is K022600.
When did POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 2002-09-16, under 510(k) number K022600.
Who is the listed applicant for POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES?
The FDA 510(k) record lists Shijiazhuang Wally Plastics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES?
The FDA product code for POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVES 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 Shijiazhuang Wally Plastics 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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