Q750 ELECTROCARDIOGRAPH— 510(k) K885000

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K885000 for Q750 ELECTROCARDIOGRAPH, Substantially Equivalent on 1989-02-23. Applicant: Quinton, Inc..

Clearance details

Applicant: Quinton, Inc.
Product code: Code LOS
Advisory panel: Unknown
Date received: 1988-12-01
Decision date: 1989-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Quinton, Inc.

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