SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED
K-Number: K060784 · 2006-05-01
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Device Summary
Frequently Asked Questions
What is the SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED?
SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED is a medical device that received FDA 510(k) clearance on 2006-05-01. The listed applicant is Ever Light Plastic Products Co., Ltd.. The 510(k) number is K060784.
When did SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED receive FDA 510(k) clearance?
SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED received FDA 510(k) clearance on 2006-05-01, under 510(k) number K060784.
Who is the listed applicant for SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED?
The FDA 510(k) record lists Ever Light Plastic Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED?
The FDA product code for SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED 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 Ever Light Plastic Products 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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