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FDA 510(k)

SAFE-DWELL PLUS CENTRAL VENOUS CATHETER

K-Number: K921270 · 1992-09-28

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1992-09-28
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

SAFE-DWELL PLUS CENTRAL VENOUS CATHETER 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 1992-09-28 under 510(k) number K921270. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SAFE-DWELL PLUS CENTRAL VENOUS CATHETER?

SAFE-DWELL PLUS CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 1992-09-28. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K921270.

When did SAFE-DWELL PLUS CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?

SAFE-DWELL PLUS CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 1992-09-28, under 510(k) number K921270.

Who is the listed applicant for SAFE-DWELL PLUS CENTRAL VENOUS CATHETER?

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 SAFE-DWELL PLUS CENTRAL VENOUS CATHETER?

The FDA product code for SAFE-DWELL PLUS CENTRAL VENOUS CATHETER is FOZ.

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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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