PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)
K-Number: K905765 · 1991-02-25
Advertisement
Device Summary
Frequently Asked Questions
What is the PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)?
PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES) is a medical device that received FDA 510(k) clearance on 1991-02-25. The listed applicant is Tillotson Rubber Co., Inc.. The 510(k) number is K905765.
When did PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES) receive FDA 510(k) clearance?
PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES) received FDA 510(k) clearance on 1991-02-25, under 510(k) number K905765.
Who is the listed applicant for PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)?
The FDA 510(k) record lists Tillotson Rubber Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)?
The FDA product code for PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES) 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 Tillotson Rubber Co., 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.
Advertisement