RUBBERCARE LOPRO PATIENT EXAMINATION GLOVES, POWDERED
K-Number: K933759 · 1994-03-21
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Device Summary
Frequently Asked Questions
What is the RUBBERCARE LOPRO PATIENT EXAMINATION GLOVES, POWDERED?
RUBBERCARE LOPRO PATIENT EXAMINATION GLOVES, POWDERED is a medical device that received FDA 510(k) clearance on 1994-03-21. The listed applicant is Perusahaan Pelindung Getah (M) Sdn Bhd. The 510(k) number is K933759.
When did RUBBERCARE LOPRO PATIENT EXAMINATION GLOVES, POWDERED receive FDA 510(k) clearance?
RUBBERCARE LOPRO PATIENT EXAMINATION GLOVES, POWDERED received FDA 510(k) clearance on 1994-03-21, under 510(k) number K933759.
Who is the listed applicant for RUBBERCARE LOPRO PATIENT EXAMINATION GLOVES, POWDERED?
The FDA 510(k) record lists Perusahaan Pelindung Getah (M) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RUBBERCARE LOPRO PATIENT EXAMINATION GLOVES, POWDERED?
The FDA product code for RUBBERCARE LOPRO PATIENT EXAMINATION GLOVES, POWDERED 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 Perusahaan Pelindung Getah (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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