NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDERED
K-Number: K984309 · 1999-02-12
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Device Summary
Frequently Asked Questions
What is the NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDERED?
NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDERED is a medical device that received FDA 510(k) clearance on 1999-02-12. The listed applicant is Sumirubber Industries (Kedah) Sdn. Bhd.. The 510(k) number is K984309.
When did NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDERED receive FDA 510(k) clearance?
NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDERED received FDA 510(k) clearance on 1999-02-12, under 510(k) number K984309.
Who is the listed applicant for NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDERED?
The FDA 510(k) record lists Sumirubber Industries (Kedah) Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDERED?
The FDA product code for NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDERED 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 Sumirubber Industries (Kedah) 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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