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FDA 510(k)

L3 (LEAD LATEX LYSNIG GLOVES)

K-Number: K882437 · 1989-05-11

ApplicantThe Branford Co.
Decision Date1989-05-11
Product CodeLZC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

L3 (LEAD LATEX LYSNIG GLOVES) is the device name listed in this FDA 510(k) record. The listed applicant is The Branford Co.. It received FDA 510(k) clearance on 1989-05-11 under 510(k) number K882437. The device is classified under product code LZC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L3 (LEAD LATEX LYSNIG GLOVES)?

L3 (LEAD LATEX LYSNIG GLOVES) is a medical device that received FDA 510(k) clearance on 1989-05-11. The listed applicant is The Branford Co.. The 510(k) number is K882437.

When did L3 (LEAD LATEX LYSNIG GLOVES) receive FDA 510(k) clearance?

L3 (LEAD LATEX LYSNIG GLOVES) received FDA 510(k) clearance on 1989-05-11, under 510(k) number K882437.

Who is the listed applicant for L3 (LEAD LATEX LYSNIG GLOVES)?

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

What is the FDA product code for L3 (LEAD LATEX LYSNIG GLOVES)?

The FDA product code for L3 (LEAD LATEX LYSNIG GLOVES) is LZC.

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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.

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