POWDERFREE BLACK NITRILE EXAMINATION GLOVES
K-Number: K102620 · 2010-11-22
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Device Summary
Frequently Asked Questions
What is the POWDERFREE BLACK NITRILE EXAMINATION GLOVES?
POWDERFREE BLACK NITRILE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2010-11-22. The listed applicant is Pt. Medisafe Technologies. The 510(k) number is K102620.
When did POWDERFREE BLACK NITRILE EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDERFREE BLACK NITRILE EXAMINATION GLOVES received FDA 510(k) clearance on 2010-11-22, under 510(k) number K102620.
Who is the listed applicant for POWDERFREE BLACK NITRILE EXAMINATION GLOVES?
The FDA 510(k) record lists Pt. Medisafe Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDERFREE BLACK NITRILE EXAMINATION GLOVES?
The FDA product code for POWDERFREE BLACK NITRILE EXAMINATION GLOVES is LZA.
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 Pt. Medisafe Technologies 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: LZA)
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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