SPIROVISION— 510(k) K864885

Name: FDA 510(k) clearance K864885
Creator: U.S. Food and Drug Administration
Published: 1987-01-15

Substantially Equivalent

Futuremed Div. of Future Impex Corp.

FDA 510(k) clearance K864885 for SPIROVISION, Substantially Equivalent on 1987-01-15. Applicant: Futuremed Div. of Future Impex Corp.. Device class: 2.

Clearance details

Applicant: Futuremed Div. of Future Impex Corp.
Product code: Code BZM
Device class: Class 2
Regulation: 21 CFR 868.1900
Advisory panel: Anesthesiology
Date received: 1986-12-12
Decision date: 1987-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deerpark, NY, US

Download summary PDF View on FDA.gov ↗

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