VINYL EXAMINATION GLOVE, POWDER FREE
K-Number: K941357 · 1994-04-29
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Device Summary
Frequently Asked Questions
What is the VINYL EXAMINATION GLOVE, POWDER FREE?
VINYL EXAMINATION GLOVE, POWDER FREE is a medical device that received FDA 510(k) clearance on 1994-04-29. The listed applicant is Canopus Medical Supply Co., Ltd.. The 510(k) number is K941357.
When did VINYL EXAMINATION GLOVE, POWDER FREE receive FDA 510(k) clearance?
VINYL EXAMINATION GLOVE, POWDER FREE received FDA 510(k) clearance on 1994-04-29, under 510(k) number K941357.
Who is the listed applicant for VINYL EXAMINATION GLOVE, POWDER FREE?
The FDA 510(k) record lists Canopus Medical Supply Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINYL EXAMINATION GLOVE, POWDER FREE?
The FDA product code for VINYL EXAMINATION GLOVE, POWDER FREE 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 Canopus Medical Supply 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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