FDA 510(k)

MULTIPLE NAME

K-Number: K103337 · 2011-02-25

Decision Date2011-02-25

Product CodeLZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MULTIPLE NAME is the device name listed in this FDA 510(k) record. The listed applicant is Ideal Quality Sdn., Bhd.. It received FDA 510(k) clearance on 2011-02-25 under 510(k) number K103337. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE NAME?

MULTIPLE NAME is a medical device that received FDA 510(k) clearance on 2011-02-25. The listed applicant is Ideal Quality Sdn., Bhd.. The 510(k) number is K103337.

When did MULTIPLE NAME receive FDA 510(k) clearance?

MULTIPLE NAME received FDA 510(k) clearance on 2011-02-25, under 510(k) number K103337.

Who is the listed applicant for MULTIPLE NAME?

The FDA 510(k) record lists Ideal Quality Sdn., Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIPLE NAME?

The FDA product code for MULTIPLE NAME is LZA.

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Other records listing Ideal Quality Sdn., Bhd. as applicant

K981062POLYMER COATED, POWDER-FREE LATEX EXAMINATION GLOVES K974662POWDER-FREE LATEX EXAMINATION GLOVE K974660LATEX EXAMINATION GLOVE

Related Devices (Code: LZA)

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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.