POWDERFREE GREEN NITRILE EXAMINATION GLOVES
K-Number: K974887 · 1998-01-29
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Device Summary
Frequently Asked Questions
What is the POWDERFREE GREEN NITRILE EXAMINATION GLOVES?
POWDERFREE GREEN NITRILE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1998-01-29. The listed applicant is Sri Johani Sdn. Bhd.. The 510(k) number is K974887.
When did POWDERFREE GREEN NITRILE EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDERFREE GREEN NITRILE EXAMINATION GLOVES received FDA 510(k) clearance on 1998-01-29, under 510(k) number K974887.
Who is the listed applicant for POWDERFREE GREEN NITRILE EXAMINATION GLOVES?
The FDA 510(k) record lists Sri Johani Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDERFREE GREEN NITRILE EXAMINATION GLOVES?
The FDA product code for POWDERFREE GREEN 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 Sri Johani 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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