DeviceClearance

LEAD CONVERSION KIT, MODEL 341— 510(k) K781111

Substantially Equivalent

Edwards Pacemaker Systems

FDA 510(k) clearance K781111 for LEAD CONVERSION KIT, MODEL 341, Substantially Equivalent on 1978-08-31. Applicant: Edwards Pacemaker Systems.

Clearance details

Applicant
Edwards Pacemaker Systems
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

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