FDA 510(k)

STRAWBERRY SCENTED LATEX EXAMINATION GLOVES

K-Number: K896135 · 1989-12-01

ApplicantArista Latindo Industrial Ltd. P.T

Decision Date1989-12-01

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

STRAWBERRY SCENTED LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Arista Latindo Industrial Ltd. P.T. It received FDA 510(k) clearance on 1989-12-01 under 510(k) number K896135. 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 STRAWBERRY SCENTED LATEX EXAMINATION GLOVES?

STRAWBERRY SCENTED LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-12-01. The listed applicant is Arista Latindo Industrial Ltd. P.T. The 510(k) number is K896135.

When did STRAWBERRY SCENTED LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?

STRAWBERRY SCENTED LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-12-01, under 510(k) number K896135.

Who is the listed applicant for STRAWBERRY SCENTED LATEX EXAMINATION GLOVES?

The FDA 510(k) record lists Arista Latindo Industrial Ltd. P.T as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRAWBERRY SCENTED LATEX EXAMINATION GLOVES?

The FDA product code for STRAWBERRY SCENTED LATEX EXAMINATION GLOVES is LYY.

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Related Devices (Code: LYY)

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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.