QUINTON MEDTRACK CR PLUS TREADMILL— 510(k) K990866

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K990866 for QUINTON MEDTRACK CR PLUS TREADMILL, Substantially Equivalent on 1999-04-29. Applicant: Quinton, Inc..

Clearance details

Applicant: Quinton, Inc.
Product code: Code ISD
Advisory panel: Physical Medicine
Date received: 1999-03-16
Decision date: 1999-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

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Adverse events under product code ISD

product code ISD

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.