ROSENTHAL-FRENCH NEBULIZATION DOSIMETER— 510(k) K860800

Name: FDA 510(k) clearance K860800
Creator: U.S. Food and Drug Administration
Published: 1986-03-27

Substantially Equivalent

Laboratory For Applied Immunology, Inc.

FDA 510(k) clearance K860800 for ROSENTHAL-FRENCH NEBULIZATION DOSIMETER, Substantially Equivalent on 1986-03-27. Applicant: Laboratory For Applied Immunology, Inc.. Device class: 1.

Clearance details

Applicant: Laboratory For Applied Immunology, Inc.
Product code: Code CCQ
Device class: Class 1
Regulation: 21 CFR 868.5640
Advisory panel: Anesthesiology
Date received: 1986-03-04
Decision date: 1986-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairfax, VA, US

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