TEMPORARY SCREENING LEAD/ CATHETER KIT— 510(k) K934939

Name: FDA 510(k) clearance K934939
Creator: U.S. Food and Drug Administration
Published: 1995-05-24

Substantially Equivalent

Medtronic Vascular

FDA 510(k) clearance K934939 for TEMPORARY SCREENING LEAD/ CATHETER KIT, Substantially Equivalent on 1995-05-24. Applicant: Medtronic Vascular. Device class: 2.

Clearance details

Applicant: Medtronic Vascular
Product code: Code MAJ
Device class: Class 2
Regulation: 21 CFR 868.5120
Advisory panel: Anesthesiology
Date received: 1993-10-18
Decision date: 1995-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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