KOKO SPIROMETER— 510(k) K914272

Substantially Equivalent

Ferraris Respiratory, Inc.

FDA 510(k) clearance K914272 for KOKO SPIROMETER, Substantially Equivalent on 1992-07-02. Applicant: Ferraris Respiratory, Inc.. Device class: 2.

Clearance details

Applicant: Ferraris Respiratory, Inc.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1991-09-24
Decision date: 1992-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Louisville, CO, US

Download summary PDF View on FDA.gov ↗

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