ARG LATEX EXAMINATION GLOVES
K-Number: K891510 · 1989-04-28
Advertisement
Device Summary
Frequently Asked Questions
What is the ARG LATEX EXAMINATION GLOVES?
ARG LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-28. The listed applicant is Palmbase Rubber Mfg. (M) Sdn Bhd. The 510(k) number is K891510.
When did ARG LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
ARG LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-04-28, under 510(k) number K891510.
Who is the listed applicant for ARG LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Palmbase Rubber Mfg. (M) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARG LATEX EXAMINATION GLOVES?
The FDA product code for ARG LATEX 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.
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.
Advertisement