PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER
K-Number: K893782 · 1989-07-14
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER?
PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Rubberex (M) Sdn Berhad. The 510(k) number is K893782.
When did PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER receive FDA 510(k) clearance?
PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893782.
Who is the listed applicant for PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER?
The FDA 510(k) record lists Rubberex (M) Sdn Berhad as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER?
The FDA product code for PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER 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 Rubberex (M) Sdn Berhad 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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