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FDA 510(k)

STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES

K-Number: K000891 · 2000-04-28

Decision Date2000-04-28
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Fitco Dipped Products Pvt., Ltd.. It received FDA 510(k) clearance on 2000-04-28 under 510(k) number K000891. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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