MODEL 6888 LEAD TUNNELER— 510(k) K894738

Name: FDA 510(k) clearance K894738
Creator: U.S. Food and Drug Administration
Published: 1989-09-13

Substantially Equivalent

Cardiac Pacemakers, Inc.

FDA 510(k) clearance K894738 for MODEL 6888 LEAD TUNNELER, Substantially Equivalent on 1989-09-13. Applicant: Cardiac Pacemakers, Inc.. Device class: 1.

Clearance details

Applicant: Cardiac Pacemakers, Inc.
Product code: Code DWS
Device class: Class 1
Regulation: 21 CFR 870.4500
Advisory panel: Cardiovascular
Date received: 1989-07-27
Decision date: 1989-09-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, 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.