HWA (AND) SILKTEX PRE-POWDERED LATEX EXAMINATION GLOVE
K-Number: K992730 · 1999-09-14
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Device Summary
Frequently Asked Questions
What is the HWA (AND) SILKTEX PRE-POWDERED LATEX EXAMINATION GLOVE?
HWA (AND) SILKTEX PRE-POWDERED LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1999-09-14. The listed applicant is Hwa Teh Industrial Sdn. Bhd.. The 510(k) number is K992730.
When did HWA (AND) SILKTEX PRE-POWDERED LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?
HWA (AND) SILKTEX PRE-POWDERED LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1999-09-14, under 510(k) number K992730.
Who is the listed applicant for HWA (AND) SILKTEX PRE-POWDERED LATEX EXAMINATION GLOVE?
The FDA 510(k) record lists Hwa Teh Industrial Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HWA (AND) SILKTEX PRE-POWDERED LATEX EXAMINATION GLOVE?
The FDA product code for HWA (AND) SILKTEX PRE-POWDERED LATEX EXAMINATION GLOVE 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 Hwa Teh Industrial 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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