B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.— 510(k) K915480

Name: FDA 510(k) clearance K915480
Creator: U.S. Food and Drug Administration
Published: 1992-01-07

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K915480 for B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT., Substantially Equivalent on 1992-01-07. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code DWD
Device class: Class 2
Regulation: 21 CFR 870.4430
Advisory panel: Cardiovascular
Date received: 1991-12-06
Decision date: 1992-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin Lakes, NJ, US

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