FREEFORM BLUE POWDERFREE NITRILE EXAMINATION GLOVES
K-Number: K022671 · 2002-11-18
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Device Summary
Frequently Asked Questions
What is the FREEFORM BLUE POWDERFREE NITRILE EXAMINATION GLOVES?
FREEFORM BLUE POWDERFREE NITRILE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2002-11-18. The listed applicant is Hartalega Sdn Bhd. The 510(k) number is K022671.
When did FREEFORM BLUE POWDERFREE NITRILE EXAMINATION GLOVES receive FDA 510(k) clearance?
FREEFORM BLUE POWDERFREE NITRILE EXAMINATION GLOVES received FDA 510(k) clearance on 2002-11-18, under 510(k) number K022671.
Who is the listed applicant for FREEFORM BLUE POWDERFREE NITRILE EXAMINATION GLOVES?
The FDA 510(k) record lists Hartalega Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FREEFORM BLUE POWDERFREE NITRILE EXAMINATION GLOVES?
The FDA product code for FREEFORM BLUE POWDERFREE 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 Hartalega Sdn Bhd 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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