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FDA 510(k)

B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT

K-Number: K915482 · 1992-01-07

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1992-01-07
Product CodeDWD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT 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 1992-01-07 under 510(k) number K915482. The device is classified under product code DWD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT?

B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT is a medical device that received FDA 510(k) clearance on 1992-01-07. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K915482.

When did B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT receive FDA 510(k) clearance?

B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT received FDA 510(k) clearance on 1992-01-07, under 510(k) number K915482.

Who is the listed applicant for B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT?

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 B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT?

The FDA product code for B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT is DWD.

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Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic as applicant

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Related Devices (Code: DWD)

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.

K992657IBC VRV, MODEL 1350International Biophysics Corp.K920077NIKKISO NK PUMPInternational Medical Products, Inc.K915480B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.Bd Becton Dickinson Vacutainer Systems PreanalyticK915481B-D ULTRA-VUE PROCEDURE NEEDLE W/ CHIBA TYPE POINTBd Becton Dickinson Vacutainer Systems PreanalyticK905311DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.Baxter Bentley Laboratories, Inc.K895427MEDISEAL SUCTION CANISTERDeroyal Industries, Inc.

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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