PACESETTER SYSTEMS, INC. ENDOCARDIAL SCREW-IN LEAD— 510(k) K844857

Substantially Equivalent

Pacesetter Systems

FDA 510(k) clearance K844857 for PACESETTER SYSTEMS, INC. ENDOCARDIAL SCREW-IN LEAD, Substantially Equivalent on 1985-02-14. Applicant: Pacesetter Systems.

Clearance details

Applicant: Pacesetter Systems
Product code: Code DTD
Advisory panel: Cardiovascular
Date received: 1984-12-14
Decision date: 1985-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sylmar, CA, US

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