Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

POWDERED PATIENT EXAMINATION GLOVES, LATEX

K-Number: K001715 · 2000-07-05

Decision Date2000-07-05
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDERED PATIENT EXAMINATION GLOVES, LATEX 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 2000-07-05 under 510(k) number K001715. 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 POWDERED PATIENT EXAMINATION GLOVES, LATEX?

POWDERED PATIENT EXAMINATION GLOVES, LATEX is a medical device that received FDA 510(k) clearance on 2000-07-05. The listed applicant is Fitco Dipped Products Pvt., Ltd.. The 510(k) number is K001715.

When did POWDERED PATIENT EXAMINATION GLOVES, LATEX receive FDA 510(k) clearance?

POWDERED PATIENT EXAMINATION GLOVES, LATEX received FDA 510(k) clearance on 2000-07-05, under 510(k) number K001715.

Who is the listed applicant for POWDERED PATIENT EXAMINATION GLOVES, LATEX?

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 POWDERED PATIENT EXAMINATION GLOVES, LATEX?

The FDA product code for POWDERED PATIENT EXAMINATION GLOVES, LATEX 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.

↑