CIRRUS NEBULIZER-DELUXE KIT— 510(k) K854952

Name: FDA 510(k) clearance K854952
Creator: U.S. Food and Drug Administration
Published: 1986-01-28

Substantially Equivalent

Dhd Medical Products Div. Diemolding Corp.

FDA 510(k) clearance K854952 for CIRRUS NEBULIZER-DELUXE KIT, Substantially Equivalent on 1986-01-28. Applicant: Dhd Medical Products Div. Diemolding Corp.. Device class: 1.

Clearance details

Applicant: Dhd Medical Products Div. Diemolding Corp.
Product code: Code CCQ
Device class: Class 1
Regulation: 21 CFR 868.5640
Advisory panel: Anesthesiology
Date received: 1985-12-10
Decision date: 1986-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canastota, NY, US

Download summary PDF View on FDA.gov ↗

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