MAESTRO PACEMAKER TEST MAGNET— 510(k) K895110

Name: FDA 510(k) clearance K895110
Creator: U.S. Food and Drug Administration
Published: 1989-09-26

Substantially Equivalent

Cardiac Control Systems, Inc.

FDA 510(k) clearance K895110 for MAESTRO PACEMAKER TEST MAGNET, Substantially Equivalent on 1989-09-26. Applicant: Cardiac Control Systems, Inc.. Device class: 1.

Clearance details

Applicant: Cardiac Control Systems, Inc.
Product code: Code DTG
Device class: Class 1
Regulation: 21 CFR 870.3690
Advisory panel: Cardiovascular
Date received: 1989-08-15
Decision date: 1989-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palm Coast, FL, US

Download summary PDF View on FDA.gov ↗

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K923868 — CCS MAESTRO II SERIES 200 CARDIAC PACEMAKER1993-05-14
K905824 — MAESTRO(R) SERIES 100/200 CARDIAC S/CHAMB PACEMAKE1991-05-16

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