DISPOSABLE NON STERILE LATEX EXAM GLOVES
K-Number: K890905 · 1989-08-31
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE NON STERILE LATEX EXAM GLOVES?
DISPOSABLE NON STERILE LATEX EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-31. The listed applicant is Harvest Intl. of America, Inc.. The 510(k) number is K890905.
When did DISPOSABLE NON STERILE LATEX EXAM GLOVES receive FDA 510(k) clearance?
DISPOSABLE NON STERILE LATEX EXAM GLOVES received FDA 510(k) clearance on 1989-08-31, under 510(k) number K890905.
Who is the listed applicant for DISPOSABLE NON STERILE LATEX EXAM GLOVES?
The FDA 510(k) record lists Harvest Intl. of America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE NON STERILE LATEX EXAM GLOVES?
The FDA product code for DISPOSABLE NON STERILE LATEX EXAM 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.
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