PVC VINYL GLOVE
K-Number: K910891 · 1991-03-11
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Device Summary
Frequently Asked Questions
What is the PVC VINYL GLOVE?
PVC VINYL GLOVE is a medical device that received FDA 510(k) clearance on 1991-03-11. The listed applicant is Pioneer Sundries Products , Ltd.. The 510(k) number is K910891.
When did PVC VINYL GLOVE receive FDA 510(k) clearance?
PVC VINYL GLOVE received FDA 510(k) clearance on 1991-03-11, under 510(k) number K910891.
Who is the listed applicant for PVC VINYL GLOVE?
The FDA 510(k) record lists Pioneer Sundries Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PVC VINYL GLOVE?
The FDA product code for PVC VINYL 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 Pioneer Sundries Products , 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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