PROLAX DISPOSABLE LATEX GLOVES (PROCEDURE STERILE)
K-Number: K903351 · 1990-09-26
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Device Summary
Frequently Asked Questions
What is the PROLAX DISPOSABLE LATEX GLOVES (PROCEDURE STERILE)?
PROLAX DISPOSABLE LATEX GLOVES (PROCEDURE STERILE) is a medical device that received FDA 510(k) clearance on 1990-09-26. The listed applicant is Prolax Medical Products, Inc.. The 510(k) number is K903351.
When did PROLAX DISPOSABLE LATEX GLOVES (PROCEDURE STERILE) receive FDA 510(k) clearance?
PROLAX DISPOSABLE LATEX GLOVES (PROCEDURE STERILE) received FDA 510(k) clearance on 1990-09-26, under 510(k) number K903351.
Who is the listed applicant for PROLAX DISPOSABLE LATEX GLOVES (PROCEDURE STERILE)?
The FDA 510(k) record lists Prolax Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROLAX DISPOSABLE LATEX GLOVES (PROCEDURE STERILE)?
The FDA product code for PROLAX DISPOSABLE LATEX GLOVES (PROCEDURE STERILE) 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 Prolax Medical Products, Inc. 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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