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FDA 510(k)

FEATHERWEIGHT VINYL, NON-STERILE EXAM GLOVES

K-Number: K892328 · 1989-12-05

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1989-12-05
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FEATHERWEIGHT VINYL, NON-STERILE EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1989-12-05 under 510(k) number K892328. 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 FEATHERWEIGHT VINYL, NON-STERILE EXAM GLOVES?

FEATHERWEIGHT VINYL, NON-STERILE EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-12-05. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K892328.

When did FEATHERWEIGHT VINYL, NON-STERILE EXAM GLOVES receive FDA 510(k) clearance?

FEATHERWEIGHT VINYL, NON-STERILE EXAM GLOVES received FDA 510(k) clearance on 1989-12-05, under 510(k) number K892328.

Who is the listed applicant for FEATHERWEIGHT VINYL, NON-STERILE EXAM GLOVES?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FEATHERWEIGHT VINYL, NON-STERILE EXAM GLOVES?

The FDA product code for FEATHERWEIGHT VINYL, NON-STERILE EXAM GLOVES is LYZ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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