POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVE
K-Number: K111598 · 2011-07-20
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Device Summary
Frequently Asked Questions
What is the POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVE?
POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2011-07-20. The listed applicant is Lpl (Hui Zhou) Glove Co., Ltd.. The 510(k) number is K111598.
When did POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVE receive FDA 510(k) clearance?
POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVE received FDA 510(k) clearance on 2011-07-20, under 510(k) number K111598.
Who is the listed applicant for POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVE?
The FDA 510(k) record lists Lpl (Hui Zhou) Glove Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVE?
The FDA product code for POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVE 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.
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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