LATEX PATIENT EXAMINATION GLOVES
K-Number: K924357 · 1994-02-03
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Device Summary
Frequently Asked Questions
What is the LATEX PATIENT EXAMINATION GLOVES?
LATEX PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1994-02-03. The listed applicant is Asia Pacific Latex Sdn Bhd. The 510(k) number is K924357.
When did LATEX PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
LATEX PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1994-02-03, under 510(k) number K924357.
Who is the listed applicant for LATEX PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Asia Pacific Latex Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX PATIENT EXAMINATION GLOVES?
The FDA product code for LATEX PATIENT EXAMINATION GLOVES 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 Asia Pacific Latex 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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