PATIENT EXAMINATION GLOVES (POWDER FREE)
K-Number: K932116 · 1994-03-15
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAMINATION GLOVES (POWDER FREE)?
PATIENT EXAMINATION GLOVES (POWDER FREE) is a medical device that received FDA 510(k) clearance on 1994-03-15. The listed applicant is Evergrade Healthcare Products Sdn Bhd. The 510(k) number is K932116.
When did PATIENT EXAMINATION GLOVES (POWDER FREE) receive FDA 510(k) clearance?
PATIENT EXAMINATION GLOVES (POWDER FREE) received FDA 510(k) clearance on 1994-03-15, under 510(k) number K932116.
Who is the listed applicant for PATIENT EXAMINATION GLOVES (POWDER FREE)?
The FDA 510(k) record lists Evergrade Healthcare Products Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAMINATION GLOVES (POWDER FREE)?
The FDA product code for PATIENT EXAMINATION GLOVES (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 Evergrade Healthcare Products 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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