POWDER-FREE VINYL PATIENT EXAMINTION GLOVES
K-Number: K042119 · 2004-11-03
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Device Summary
Frequently Asked Questions
What is the POWDER-FREE VINYL PATIENT EXAMINTION GLOVES?
POWDER-FREE VINYL PATIENT EXAMINTION GLOVES is a medical device that received FDA 510(k) clearance on 2004-11-03. The listed applicant is Shijiazhuang Manful Light Industrial Products Co.,. The 510(k) number is K042119.
When did POWDER-FREE VINYL PATIENT EXAMINTION GLOVES receive FDA 510(k) clearance?
POWDER-FREE VINYL PATIENT EXAMINTION GLOVES received FDA 510(k) clearance on 2004-11-03, under 510(k) number K042119.
Who is the listed applicant for POWDER-FREE VINYL PATIENT EXAMINTION GLOVES?
The FDA 510(k) record lists Shijiazhuang Manful Light Industrial Products Co., as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER-FREE VINYL PATIENT EXAMINTION GLOVES?
The FDA product code for POWDER-FREE VINYL PATIENT EXAMINTION 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 Manful Light Industrial Products Co., 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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