LATEX EXAM/SURGICAL GLOVES
K-Number: K920202 · 1992-07-23
Advertisement
Device Summary
Frequently Asked Questions
What is the LATEX EXAM/SURGICAL GLOVES?
LATEX EXAM/SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1992-07-23. The listed applicant is Redsun Latex , Ltd.. The 510(k) number is K920202.
When did LATEX EXAM/SURGICAL GLOVES receive FDA 510(k) clearance?
LATEX EXAM/SURGICAL GLOVES received FDA 510(k) clearance on 1992-07-23, under 510(k) number K920202.
Who is the listed applicant for LATEX EXAM/SURGICAL GLOVES?
The FDA 510(k) record lists Redsun Latex , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX EXAM/SURGICAL GLOVES?
The FDA product code for LATEX EXAM/SURGICAL 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