LAGLOVE BRAND LATEX EXAMINATION GLOVE (POWDER FREE)
K-Number: K990270 · 1999-02-18
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Device Summary
Frequently Asked Questions
What is the LAGLOVE BRAND LATEX EXAMINATION GLOVE (POWDER FREE)?
LAGLOVE BRAND LATEX EXAMINATION GLOVE (POWDER FREE) is a medical device that received FDA 510(k) clearance on 1999-02-18. The listed applicant is La Glove (M) Sdn. Bhd.. The 510(k) number is K990270.
When did LAGLOVE BRAND LATEX EXAMINATION GLOVE (POWDER FREE) receive FDA 510(k) clearance?
LAGLOVE BRAND LATEX EXAMINATION GLOVE (POWDER FREE) received FDA 510(k) clearance on 1999-02-18, under 510(k) number K990270.
Who is the listed applicant for LAGLOVE BRAND LATEX EXAMINATION GLOVE (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 LATEX EXAMINATION GLOVE (POWDER FREE)?
The FDA product code for LAGLOVE BRAND LATEX EXAMINATION GLOVE (POWDER FREE) is LYY.
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: LYY)
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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