POWDER FREE VINYL PATIENT EXAMINATION GLOVE
K-Number: K093798 · 2010-02-23
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Device Summary
Frequently Asked Questions
What is the POWDER FREE VINYL PATIENT EXAMINATION GLOVE?
POWDER FREE VINYL PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2010-02-23. The listed applicant is Supermax Plastic Products Co., Ltd.. The 510(k) number is K093798.
When did POWDER FREE VINYL PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?
POWDER FREE VINYL PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 2010-02-23, under 510(k) number K093798.
Who is the listed applicant for POWDER FREE VINYL PATIENT EXAMINATION GLOVE?
The FDA 510(k) record lists Supermax Plastic Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE VINYL PATIENT EXAMINATION GLOVE?
The FDA product code for POWDER FREE VINYL PATIENT 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.
Other records listing Supermax 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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