DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011— 510(k) K870382

Name: FDA 510(k) clearance K870382
Creator: U.S. Food and Drug Administration
Published: 1987-03-06

Substantially Equivalent

Nova-Ventrx

FDA 510(k) clearance K870382 for DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011, Substantially Equivalent on 1987-03-06. Applicant: Nova-Ventrx. Device class: 2.

Clearance details

Applicant: Nova-Ventrx
Product code: Code CBP
Device class: Class 2
Regulation: 21 CFR 868.5870
Advisory panel: Anesthesiology
Date received: 1987-01-29
Decision date: 1987-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wheeling, IL, US

Download summary PDF View on FDA.gov ↗

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