SURGIMAX PATIENT EXAM GLOVES (LATEX)
K-Number: K891744 · 1989-09-01
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Device Summary
Frequently Asked Questions
What is the SURGIMAX PATIENT EXAM GLOVES (LATEX)?
SURGIMAX PATIENT EXAM GLOVES (LATEX) is a medical device that received FDA 510(k) clearance on 1989-09-01. The listed applicant is Excel Rubber Products (M) Sdn. Bhd.. The 510(k) number is K891744.
When did SURGIMAX PATIENT EXAM GLOVES (LATEX) receive FDA 510(k) clearance?
SURGIMAX PATIENT EXAM GLOVES (LATEX) received FDA 510(k) clearance on 1989-09-01, under 510(k) number K891744.
Who is the listed applicant for SURGIMAX PATIENT EXAM GLOVES (LATEX)?
The FDA 510(k) record lists Excel Rubber Products (M) Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGIMAX PATIENT EXAM GLOVES (LATEX)?
The FDA product code for SURGIMAX PATIENT EXAM GLOVES (LATEX) 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.
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