Q101 DIAGNOSTIC SPIROMETER— 510(k) K863300

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K863300 for Q101 DIAGNOSTIC SPIROMETER, Substantially Equivalent on 1986-11-13. Applicant: Quinton, Inc..

Clearance details

Applicant: Quinton, Inc.
Product code: Code BYT
Advisory panel: Anesthesiology
Date received: 1986-08-25
Decision date: 1986-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

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