LEAD EXTENDER MODEL 6516— 510(k) K770199

Substantially Equivalent

Cardiac Pacemakers, Inc.

FDA 510(k) clearance K770199 for LEAD EXTENDER MODEL 6516, Substantially Equivalent on 1977-02-07. Applicant: Cardiac Pacemakers, Inc..

Clearance details

Applicant: Cardiac Pacemakers, Inc.
Product code: Code DTD
Advisory panel: Cardiovascular
Date received: 1977-01-31
Decision date: 1977-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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