POWDER FREE, NON-STERILE EXAMINATION GLOVES
K-Number: K903607 · 1990-08-17
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Device Summary
Frequently Asked Questions
What is the POWDER FREE, NON-STERILE EXAMINATION GLOVES?
POWDER FREE, NON-STERILE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1990-08-17. The listed applicant is Tillotson Rubber Co., Inc.. The 510(k) number is K903607.
When did POWDER FREE, NON-STERILE EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDER FREE, NON-STERILE EXAMINATION GLOVES received FDA 510(k) clearance on 1990-08-17, under 510(k) number K903607.
Who is the listed applicant for POWDER FREE, NON-STERILE EXAMINATION GLOVES?
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 POWDER FREE, NON-STERILE EXAMINATION GLOVES?
The FDA product code for POWDER FREE, NON-STERILE EXAMINATION 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.
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.
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