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FDA 510(k)

LATEX SURGICAL GLOVES

K-Number: K890019 · 1990-02-27

ApplicantArgos S.A.
Decision Date1990-02-27
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Argos S.A.. It received FDA 510(k) clearance on 1990-02-27 under 510(k) number K890019. 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 LATEX SURGICAL GLOVES?

LATEX SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1990-02-27. The listed applicant is Argos S.A.. The 510(k) number is K890019.

When did LATEX SURGICAL GLOVES receive FDA 510(k) clearance?

LATEX SURGICAL GLOVES received FDA 510(k) clearance on 1990-02-27, under 510(k) number K890019.

Who is the listed applicant for LATEX SURGICAL GLOVES?

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

What is the FDA product code for LATEX SURGICAL GLOVES?

The FDA product code for LATEX SURGICAL GLOVES is LYZ.

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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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