POWDER-FREE VINYL EXAMINATION GLOVES
K-Number: K894686 · 1990-01-26
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Device Summary
Frequently Asked Questions
What is the POWDER-FREE VINYL EXAMINATION GLOVES?
POWDER-FREE VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is Dynarex Corp.. The 510(k) number is K894686.
When did POWDER-FREE VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDER-FREE VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 1990-01-26, under 510(k) number K894686.
Who is the listed applicant for POWDER-FREE VINYL EXAMINATION GLOVES?
The FDA 510(k) record lists Dynarex Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER-FREE VINYL EXAMINATION GLOVES?
The FDA product code for POWDER-FREE VINYL EXAMINATION GLOVES is LYY.
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 Dynarex Corp. 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: LYY)
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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