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FDA 510(k)

LATEX EXAMINATION GLOVES

K-Number: K893299 · 1989-08-10

ApplicantWestmark Sps, Inc.
Decision Date1989-08-10
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Westmark Sps, Inc.. It received FDA 510(k) clearance on 1989-08-10 under 510(k) number K893299. 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 LATEX EXAMINATION GLOVES?

LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-10. The listed applicant is Westmark Sps, Inc.. The 510(k) number is K893299.

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

LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-08-10, under 510(k) number K893299.

Who is the listed applicant for LATEX EXAMINATION GLOVES?

The FDA 510(k) record lists Westmark Sps, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX EXAMINATION GLOVES?

The FDA product code for LATEX EXAMINATION GLOVES is LYY.

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Related Devices (Code: LYY)

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.

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Official Source

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