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FDA 510(k)

HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE

K-Number: K000351 · 2000-06-23

Decision Date2000-06-23
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE is the device name listed in this FDA 510(k) record. The listed applicant is Hanwella Rubber Products , Ltd.. It received FDA 510(k) clearance on 2000-06-23 under 510(k) number K000351. 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 HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE?

HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE is a medical device that received FDA 510(k) clearance on 2000-06-23. The listed applicant is Hanwella Rubber Products , Ltd.. The 510(k) number is K000351.

When did HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE receive FDA 510(k) clearance?

HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE received FDA 510(k) clearance on 2000-06-23, under 510(k) number K000351.

Who is the listed applicant for HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE?

The FDA 510(k) record lists Hanwella Rubber Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE?

The FDA product code for HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE 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

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