UPGRADED SPIROMETER ST-90— 510(k) K933511

Name: FDA 510(k) clearance K933511
Creator: U.S. Food and Drug Administration
Published: 1994-02-10

Substantially Equivalent

Futuremed Div. of Future Impex Corp.

FDA 510(k) clearance K933511 for UPGRADED SPIROMETER ST-90, Substantially Equivalent on 1994-02-10. Applicant: Futuremed Div. of Future Impex Corp.. Device class: 2.

Clearance details

Applicant: Futuremed Div. of Future Impex Corp.
Product code: Code BTY
Device class: Class 2
Regulation: 21 CFR 868.1890
Advisory panel: Anesthesiology
Date received: 1993-07-15
Decision date: 1994-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deerpark, NY, 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.