FINESSIS POLYISOPRENE POWDERFREE SURGICAL GLOVES
K-Number: K123629 · 2013-05-13
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Device Summary
Frequently Asked Questions
What is the FINESSIS POLYISOPRENE POWDERFREE SURGICAL GLOVES?
FINESSIS POLYISOPRENE POWDERFREE SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 2013-05-13. The listed applicant is Lucenxia Prescience AG. The 510(k) number is K123629.
When did FINESSIS POLYISOPRENE POWDERFREE SURGICAL GLOVES receive FDA 510(k) clearance?
FINESSIS POLYISOPRENE POWDERFREE SURGICAL GLOVES received FDA 510(k) clearance on 2013-05-13, under 510(k) number K123629.
Who is the listed applicant for FINESSIS POLYISOPRENE POWDERFREE SURGICAL GLOVES?
The FDA 510(k) record lists Lucenxia Prescience AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FINESSIS POLYISOPRENE POWDERFREE SURGICAL GLOVES?
The FDA product code for FINESSIS POLYISOPRENE POWDERFREE 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 Lucenxia Prescience AG 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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