C.P.R. LANDMARC— 510(k) K900415

Name: FDA 510(k) clearance K900415
Creator: U.S. Food and Drug Administration
Published: 1990-06-12

Substantially Equivalent

Can-Am Medical, Inc.

FDA 510(k) clearance K900415 for C.P.R. LANDMARC, Substantially Equivalent on 1990-06-12. Applicant: Can-Am Medical, Inc.. Device class: 2.

Clearance details

Applicant: Can-Am Medical, Inc.
Product code: Code LIX
Device class: Class 2
Regulation: 21 CFR 870.5210
Advisory panel: Cardiovascular
Date received: 1990-01-30
Decision date: 1990-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario P8n 1t8, CA

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LIX

product code LIX

Other: 2
Total: 2

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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