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FDA 510(k)

LANFAN POWDER-FREE VINYL EXAM GLOVES

K-Number: K072488 · 2007-10-19

Decision Date2007-10-19
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LANFAN POWDER-FREE VINYL EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Lanfan Co., Ltd.. It received FDA 510(k) clearance on 2007-10-19 under 510(k) number K072488. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANFAN POWDER-FREE VINYL EXAM GLOVES?

LANFAN POWDER-FREE VINYL EXAM GLOVES is a medical device that received FDA 510(k) clearance on 2007-10-19. The listed applicant is Shanghai Lanfan Co., Ltd.. The 510(k) number is K072488.

When did LANFAN POWDER-FREE VINYL EXAM GLOVES receive FDA 510(k) clearance?

LANFAN POWDER-FREE VINYL EXAM GLOVES received FDA 510(k) clearance on 2007-10-19, under 510(k) number K072488.

Who is the listed applicant for LANFAN POWDER-FREE VINYL EXAM GLOVES?

The FDA 510(k) record lists Shanghai Lanfan Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LANFAN POWDER-FREE VINYL EXAM GLOVES?

The FDA product code for LANFAN POWDER-FREE VINYL EXAM GLOVES is LYZ.

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: LYZ)

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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