MAYTEX LATEX EXAMINATION GLOVES, POWDERED
K-Number: K935314 · 1994-08-01
Advertisement
Device Summary
Frequently Asked Questions
What is the MAYTEX LATEX EXAMINATION GLOVES, POWDERED?
MAYTEX LATEX EXAMINATION GLOVES, POWDERED is a medical device that received FDA 510(k) clearance on 1994-08-01. The listed applicant is Maytex Corp.. The 510(k) number is K935314.
When did MAYTEX LATEX EXAMINATION GLOVES, POWDERED receive FDA 510(k) clearance?
MAYTEX LATEX EXAMINATION GLOVES, POWDERED received FDA 510(k) clearance on 1994-08-01, under 510(k) number K935314.
Who is the listed applicant for MAYTEX LATEX EXAMINATION GLOVES, POWDERED?
The FDA 510(k) record lists Maytex Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAYTEX LATEX EXAMINATION GLOVES, POWDERED?
The FDA product code for MAYTEX LATEX 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 Maytex Corp. 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.
Advertisement