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FDA 510(k)

DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS

K-Number: K935870 · 1994-02-18

Decision Date1994-02-18
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS 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 1994-02-18 under 510(k) number K935870. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS?

DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS is a medical device that received FDA 510(k) clearance on 1994-02-18. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K935870.

When did DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS receive FDA 510(k) clearance?

DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS received FDA 510(k) clearance on 1994-02-18, under 510(k) number K935870.

Who is the listed applicant for DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS?

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 DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS?

The FDA product code for DEXTREN POWDER FREE HYPOALLERG GLOVES W/O COLORANTS is KGO.

Related Clinical Trials

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.

Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic as applicant

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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Related Devices (Code: KGO)

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.

Official Source

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

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