LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDER-FREE)
K-Number: K991950 · 1999-08-12
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Device Summary
Frequently Asked Questions
What is the LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDER-FREE)?
LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDER-FREE) is a medical device that received FDA 510(k) clearance on 1999-08-12. The listed applicant is La Glove (M) Sdn. Bhd.. The 510(k) number is K991950.
When did LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDER-FREE) receive FDA 510(k) clearance?
LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDER-FREE) received FDA 510(k) clearance on 1999-08-12, under 510(k) number K991950.
Who is the listed applicant for LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDER-FREE)?
The FDA 510(k) record lists La Glove (M) Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDER-FREE)?
The FDA product code for LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDER-FREE) 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 La Glove (M) 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: 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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