FDA 510(k)

DESERET(R) INTRODUCER SET WITH VITACUFF(R) DEVICE

K-Number: K893126 · 1989-08-10

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1989-08-10

Product CodeLJS

Advisory CommitteeHO

DecisionUnknown

Device Summary

DESERET(R) INTRODUCER SET WITH VITACUFF(R) DEVICE 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 1989-08-10 under 510(k) number K893126. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DESERET(R) INTRODUCER SET WITH VITACUFF(R) DEVICE?

DESERET(R) INTRODUCER SET WITH VITACUFF(R) DEVICE is a medical device that received FDA 510(k) clearance on 1989-08-10. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K893126.

When did DESERET(R) INTRODUCER SET WITH VITACUFF(R) DEVICE receive FDA 510(k) clearance?

DESERET(R) INTRODUCER SET WITH VITACUFF(R) DEVICE received FDA 510(k) clearance on 1989-08-10, under 510(k) number K893126.

Who is the listed applicant for DESERET(R) INTRODUCER SET WITH VITACUFF(R) DEVICE?

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 DESERET(R) INTRODUCER SET WITH VITACUFF(R) DEVICE?

The FDA product code for DESERET(R) INTRODUCER SET WITH VITACUFF(R) DEVICE is LJS.

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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.