STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES
K-Number: K000891 · 2000-04-28
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Device Summary
Frequently Asked Questions
What is the STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES?
STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2000-04-28. The listed applicant is Fitco Dipped Products Pvt., Ltd.. The 510(k) number is K000891.
When did STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 2000-04-28, under 510(k) number K000891.
Who is the listed applicant for STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Fitco Dipped Products Pvt., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES?
The FDA product code for STERILE LATEX POWDERED PATIENT 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 Fitco Dipped Products Pvt., Ltd. 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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