ASTRA 2,3,4 AND 6: CHIP REVISION— 510(k) K863000

Substantially Equivalent

Cardiac Pacemakers, Inc.

FDA 510(k) clearance K863000 for ASTRA 2,3,4 AND 6: CHIP REVISION, Substantially Equivalent on 1986-08-19. Applicant: Cardiac Pacemakers, Inc..

Clearance details

Applicant: Cardiac Pacemakers, Inc.
Advisory panel: Unknown
Date received: 1986-08-08
Decision date: 1986-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

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