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FDA 510(k)

DERMACARE SYNTHETIC MEDICAL GLOVE

K-Number: K914763 · 1992-02-07

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1992-02-07
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERMACARE SYNTHETIC MEDICAL GLOVE 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 1992-02-07 under 510(k) number K914763. 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 DERMACARE SYNTHETIC MEDICAL GLOVE?

DERMACARE SYNTHETIC MEDICAL GLOVE is a medical device that received FDA 510(k) clearance on 1992-02-07. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K914763.

When did DERMACARE SYNTHETIC MEDICAL GLOVE receive FDA 510(k) clearance?

DERMACARE SYNTHETIC MEDICAL GLOVE received FDA 510(k) clearance on 1992-02-07, under 510(k) number K914763.

Who is the listed applicant for DERMACARE SYNTHETIC MEDICAL GLOVE?

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 DERMACARE SYNTHETIC MEDICAL GLOVE?

The FDA product code for DERMACARE SYNTHETIC MEDICAL GLOVE 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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