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FDA 510(k)

LAWANA PATIENT EXAMINATION GLOVES

K-Number: K894307 · 1989-08-01

ApplicantViri Imports, Inc.
Decision Date1989-08-01
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LAWANA PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Viri Imports, Inc.. It received FDA 510(k) clearance on 1989-08-01 under 510(k) number K894307. 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 LAWANA PATIENT EXAMINATION GLOVES?

LAWANA PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-01. The listed applicant is Viri Imports, Inc.. The 510(k) number is K894307.

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

LAWANA PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-08-01, under 510(k) number K894307.

Who is the listed applicant for LAWANA PATIENT EXAMINATION GLOVES?

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

What is the FDA product code for LAWANA PATIENT EXAMINATION GLOVES?

The FDA product code for LAWANA PATIENT EXAMINATION GLOVES is LYY.

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Official Source

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