DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS— 510(k) K930286

Name: FDA 510(k) clearance K930286
Creator: U.S. Food and Drug Administration
Published: 1993-06-22

Unknown

Concord/Portex

FDA 510(k) clearance K930286 for DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS, Unknown on 1993-06-22. Applicant: Concord/Portex. Device class: 1.

Clearance details

Applicant: Concord/Portex
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1993-01-21
Decision date: 1993-06-22
Decision: Unknown
Clearance type: Traditional
Location: Keene, NH, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.