PUDENDAL/LOCAL ANESTESIA BLOCK TRAY— 510(k) K880988

Name: FDA 510(k) clearance K880988
Creator: U.S. Food and Drug Administration
Published: 1988-06-01

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K880988 for PUDENDAL/LOCAL ANESTESIA BLOCK TRAY, Substantially Equivalent on 1988-06-01. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code KNE
Device class: Class 2
Regulation: 21 CFR 884.5100
Advisory panel: Obstetrics/Gynecology
Date received: 1988-03-08
Decision date: 1988-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin Lakes, NJ, US

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