MODIFIED Q-SERIES OF TREADMILLS— 510(k) K885062

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K885062 for MODIFIED Q-SERIES OF TREADMILLS, Substantially Equivalent on 1988-12-27. Applicant: Quinton, Inc.. Device class: 1.

Clearance details

Applicant: Quinton, Inc.
Product code: Code IOL
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1988-12-06
Decision date: 1988-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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