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FDA 510(k)

SENSICARE SYNTHETIC MEDICAL GLOVES

K-Number: K915478 · 1992-01-27

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1992-01-27
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SENSICARE SYNTHETIC MEDICAL 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 1992-01-27 under 510(k) number K915478. 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 SENSICARE SYNTHETIC MEDICAL GLOVES?

SENSICARE SYNTHETIC MEDICAL GLOVES is a medical device that received FDA 510(k) clearance on 1992-01-27. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K915478.

When did SENSICARE SYNTHETIC MEDICAL GLOVES receive FDA 510(k) clearance?

SENSICARE SYNTHETIC MEDICAL GLOVES received FDA 510(k) clearance on 1992-01-27, under 510(k) number K915478.

Who is the listed applicant for SENSICARE SYNTHETIC MEDICAL 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 SENSICARE SYNTHETIC MEDICAL GLOVES?

The FDA product code for SENSICARE SYNTHETIC MEDICAL 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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