EUDERMIC POWDER-FREE SURGICAL GLOVES
K-Number: K915807 · 1992-10-28
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Device Summary
Frequently Asked Questions
What is the EUDERMIC POWDER-FREE SURGICAL GLOVES?
EUDERMIC POWDER-FREE SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1992-10-28. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K915807.
When did EUDERMIC POWDER-FREE SURGICAL GLOVES receive FDA 510(k) clearance?
EUDERMIC POWDER-FREE SURGICAL GLOVES received FDA 510(k) clearance on 1992-10-28, under 510(k) number K915807.
Who is the listed applicant for EUDERMIC POWDER-FREE SURGICAL GLOVES?
The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EUDERMIC POWDER-FREE SURGICAL GLOVES?
The FDA product code for EUDERMIC POWDER-FREE SURGICAL GLOVES is KGO.
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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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: KGO)
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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