TEST MAGNET— 510(k) K813153

Substantially Equivalent

Pacesetter Systems

FDA 510(k) clearance K813153 for TEST MAGNET, Substantially Equivalent on 1981-12-02. Applicant: Pacesetter Systems.

Clearance details

Applicant: Pacesetter Systems
Product code: Code DTG
Advisory panel: Cardiovascular
Date received: 1981-11-06
Decision date: 1981-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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