FDA 510(k)

BD ANGIOGRAPHIC SYRINGE W/A ROTATING TIP

K-Number: K910873 · 1991-05-29

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1991-05-29

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

BD ANGIOGRAPHIC SYRINGE W/A ROTATING TIP 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 1991-05-29 under 510(k) number K910873. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD ANGIOGRAPHIC SYRINGE W/A ROTATING TIP?

BD ANGIOGRAPHIC SYRINGE W/A ROTATING TIP is a medical device that received FDA 510(k) clearance on 1991-05-29. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K910873.

When did BD ANGIOGRAPHIC SYRINGE W/A ROTATING TIP receive FDA 510(k) clearance?

BD ANGIOGRAPHIC SYRINGE W/A ROTATING TIP received FDA 510(k) clearance on 1991-05-29, under 510(k) number K910873.

Who is the listed applicant for BD ANGIOGRAPHIC SYRINGE W/A ROTATING TIP?

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 BD ANGIOGRAPHIC SYRINGE W/A ROTATING TIP?

The FDA product code for BD ANGIOGRAPHIC SYRINGE W/A ROTATING TIP is DXT.

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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.